Canonical Allele Identifier: CA1251304
Gene: SERPINC1 HGNC NCBI

Linked Data

dbSNP Id: rs776791729

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909747G>A , CM000663.2:g.173909747G>A GRCh38
NC_000001.10:g.173878885G>A , CM000663.1:g.173878885G>A GRCh37
NC_000001.9:g.172145508G>A NCBI36
NG_012462.1:g.12632C>T , LRG_577:g.12632C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000367698.4:c.958C>T MANE Select ENSP00000356671.3:p.Pro320Ser
ENST00000367698.3:c.958C>T ENSP00000356671.3:p.Pro320Ser
ENST00000487183.1:n.609C>T
ENST00000617423.4:c.559+2117C>T ENSP00000478688.1:n.559+2117C>T
NM_000488.3:c.958C>T , LRG_577t1:c.958C>T NP_000479.1:p.Pro320Ser
XM_005245198.2:c.814C>T XP_005245255.1:p.Pro272Ser
NM_001365052.1:c.814C>T NP_001351981.1:p.Pro272Ser
NM_000488.4:c.958C>T MANE Select NP_000479.1:p.Pro320Ser
NM_001365052.2:c.814C>T NP_001351981.1:p.Pro272Ser
NM_001386302.1:c.1081C>T NP_001373231.1:p.Pro361Ser
NM_001386303.1:c.1039C>T NP_001373232.1:p.Pro347Ser
NM_001386304.1:c.937C>T NP_001373233.1:p.Pro313Ser
NM_001386305.1:c.901C>T NP_001373234.1:p.Pro301Ser
NM_001386306.1:c.742C>T NP_001373235.1:p.Pro248Ser