Canonical Allele Identifier: CA343773673
Gene: SERPINC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909650A>C , CM000663.2:g.173909650A>C GRCh38
NC_000001.10:g.173878788A>C , CM000663.1:g.173878788A>C GRCh37
NC_000001.9:g.172145411A>C NCBI36
NG_012462.1:g.12729T>G , LRG_577:g.12729T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000367698.4:c.1055T>G MANE Select ENSP00000356671.3:p.Met352Arg
ENST00000367698.3:c.1055T>G ENSP00000356671.3:p.Met352Arg
ENST00000617423.4:c.560-2157T>G ENSP00000478688.1:n.560-2157T>G
NM_000488.3:c.1055T>G , LRG_577t1:c.1055T>G NP_000479.1:p.Met352Arg
XM_005245198.2:c.911T>G XP_005245255.1:p.Met304Arg
NM_001365052.1:c.911T>G NP_001351981.1:p.Met304Arg
NM_000488.4:c.1055T>G MANE Select NP_000479.1:p.Met352Arg
NM_001365052.2:c.911T>G NP_001351981.1:p.Met304Arg
NM_001386302.1:c.1178T>G NP_001373231.1:p.Met393Arg
NM_001386303.1:c.1136T>G NP_001373232.1:p.Met379Arg
NM_001386304.1:c.1034T>G NP_001373233.1:p.Met345Arg
NM_001386305.1:c.998T>G NP_001373234.1:p.Met333Arg
NM_001386306.1:c.839T>G NP_001373235.1:p.Met280Arg