Canonical Allele Identifier: CA343774775
Gene: SERPINC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.173879058C>A (hg19) chr1:g.173909920C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909920C>A , CM000663.2:g.173909920C>A GRCh38
NC_000001.10:g.173879058C>A , CM000663.1:g.173879058C>A GRCh37
NC_000001.9:g.172145681C>A NCBI36
NG_012462.1:g.12459G>T , LRG_577:g.12459G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.785G>T MANE Select ENSP00000356671.3:p.Ser262Ile
ENST00000367698.3:c.785G>T ENSP00000356671.3:p.Ser262Ile
ENST00000487183.1:n.436G>T
ENST00000617423.4:c.559+1944G>T ENSP00000478688.1:n.559+1944G>T
NM_000488.3:c.785G>T , LRG_577t1:c.785G>T NP_000479.1:p.Ser262Ile
XM_005245198.2:c.641G>T XP_005245255.1:p.Ser214Ile
NM_001365052.1:c.641G>T NP_001351981.1:p.Ser214Ile
NM_000488.4:c.785G>T MANE Select NP_000479.1:p.Ser262Ile
NM_001365052.2:c.641G>T NP_001351981.1:p.Ser214Ile
NM_001386302.1:c.908G>T NP_001373231.1:p.Ser303Ile
NM_001386303.1:c.866G>T NP_001373232.1:p.Ser289Ile
NM_001386304.1:c.764G>T NP_001373233.1:p.Ser255Ile
NM_001386305.1:c.763-35G>T NP_001373234.1:n.763-35G>T
NM_001386306.1:c.569G>T NP_001373235.1:p.Ser190Ile
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