Canonical Allele Identifier: CA2649174294
Gene: SERPINC1 HGNC NCBI

Linked Data

gnomAD v4: 1-173910059-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173910059C>A , CM000663.2:g.173910059C>A GRCh38
NC_000001.10:g.173879197C>A , CM000663.1:g.173879197C>A GRCh37
NC_000001.9:g.172145820C>A NCBI36
NG_012462.1:g.12320G>T , LRG_577:g.12320G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.763-117G>T MANE Select ENSP00000356671.3:n.763-117G>T
ENST00000367698.3:c.763-117G>T ENSP00000356671.3:n.763-117G>T
ENST00000487183.1:n.414-117G>T
ENST00000617423.4:c.559+1805G>T ENSP00000478688.1:n.559+1805G>T
NM_000488.3:c.763-117G>T , LRG_577t1:c.763-117G>T NP_000479.1:n.763-117G>T
XM_005245198.2:c.619-117G>T XP_005245255.1:n.619-117G>T
NM_001365052.1:c.619-117G>T NP_001351981.1:n.619-117G>T
NM_000488.4:c.763-117G>T MANE Select NP_000479.1:n.763-117G>T
NM_001365052.2:c.619-117G>T NP_001351981.1:n.619-117G>T
NM_001386302.1:c.886-117G>T NP_001373231.1:n.886-117G>T
NM_001386303.1:c.844-117G>T NP_001373232.1:n.844-117G>T
NM_001386304.1:c.742-117G>T NP_001373233.1:n.742-117G>T
NM_001386305.1:c.763-174G>T NP_001373234.1:n.763-174G>T
NM_001386306.1:c.547-117G>T NP_001373235.1:n.547-117G>T
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