Canonical Allele Identifier: CA343774091
Gene: SERPINC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909746G>C , CM000663.2:g.173909746G>C GRCh38
NC_000001.10:g.173878884G>C , CM000663.1:g.173878884G>C GRCh37
NC_000001.9:g.172145507G>C NCBI36
NG_012462.1:g.12633C>G , LRG_577:g.12633C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.959C>G MANE Select ENSP00000356671.3:p.Pro320Arg
ENST00000367698.3:c.959C>G ENSP00000356671.3:p.Pro320Arg
ENST00000487183.1:n.610C>G
ENST00000617423.4:c.559+2118C>G ENSP00000478688.1:n.559+2118C>G
NM_000488.3:c.959C>G , LRG_577t1:c.959C>G NP_000479.1:p.Pro320Arg
XM_005245198.2:c.815C>G XP_005245255.1:p.Pro272Arg
NM_001365052.1:c.815C>G NP_001351981.1:p.Pro272Arg
NM_000488.4:c.959C>G MANE Select NP_000479.1:p.Pro320Arg
NM_001365052.2:c.815C>G NP_001351981.1:p.Pro272Arg
NM_001386302.1:c.1082C>G NP_001373231.1:p.Pro361Arg
NM_001386303.1:c.1040C>G NP_001373232.1:p.Pro347Arg
NM_001386304.1:c.938C>G NP_001373233.1:p.Pro313Arg
NM_001386305.1:c.902C>G NP_001373234.1:p.Pro301Arg
NM_001386306.1:c.743C>G NP_001373235.1:p.Pro248Arg