Canonical Allele Identifier: CA1251315
Gene: SERPINC1 HGNC NCBI

Linked Data

dbSNP Id: rs201381904

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909822C>T , CM000663.2:g.173909822C>T GRCh38
NC_000001.10:g.173878960C>T , CM000663.1:g.173878960C>T GRCh37
NC_000001.9:g.172145583C>T NCBI36
NG_012462.1:g.12557G>A , LRG_577:g.12557G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000367698.4:c.883G>A MANE Select ENSP00000356671.3:p.Val295Met
ENST00000367698.3:c.883G>A ENSP00000356671.3:p.Val295Met
ENST00000487183.1:n.534G>A
ENST00000617423.4:c.559+2042G>A ENSP00000478688.1:p.=
NM_000488.3:c.883G>A , LRG_577t1:c.883G>A NP_000479.1:p.Val295Met
XM_005245198.2:c.739G>A XP_005245255.1:p.Val247Met
NM_001365052.1:c.739G>A NP_001351981.1:p.Val247Met
NM_000488.4:c.883G>A MANE Select NP_000479.1:p.Val295Met
NM_001365052.2:c.739G>A NP_001351981.1:p.Val247Met
NM_001386302.1:c.1006G>A NP_001373231.1:p.Val336Met
NM_001386303.1:c.964G>A NP_001373232.1:p.Val322Met
NM_001386304.1:c.862G>A NP_001373233.1:p.Val288Met
NM_001386305.1:c.826G>A NP_001373234.1:p.Val276Met
NM_001386306.1:c.667G>A NP_001373235.1:p.Val223Met