Canonical Allele Identifier: CA343774330
Gene: SERPINC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.173878942C>T (hg19) chr1:g.173909804C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909804C>T , CM000663.2:g.173909804C>T GRCh38
NC_000001.10:g.173878942C>T , CM000663.1:g.173878942C>T GRCh37
NC_000001.9:g.172145565C>T NCBI36
NG_012462.1:g.12575G>A , LRG_577:g.12575G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.901G>A MANE Select ENSP00000356671.3:p.Val301Met
ENST00000367698.3:c.901G>A ENSP00000356671.3:p.Val301Met
ENST00000487183.1:n.552G>A
ENST00000617423.4:c.559+2060G>A ENSP00000478688.1:n.559+2060G>A
NM_000488.3:c.901G>A , LRG_577t1:c.901G>A NP_000479.1:p.Val301Met
XM_005245198.2:c.757G>A XP_005245255.1:p.Val253Met
NM_001365052.1:c.757G>A NP_001351981.1:p.Val253Met
NM_000488.4:c.901G>A MANE Select NP_000479.1:p.Val301Met
NM_001365052.2:c.757G>A NP_001351981.1:p.Val253Met
NM_001386302.1:c.1024G>A NP_001373231.1:p.Val342Met
NM_001386303.1:c.982G>A NP_001373232.1:p.Val328Met
NM_001386304.1:c.880G>A NP_001373233.1:p.Val294Met
NM_001386305.1:c.844G>A NP_001373234.1:p.Val282Met
NM_001386306.1:c.685G>A NP_001373235.1:p.Val229Met
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