Canonical Allele Identifier: CA343772036

Gene: SERPINC1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173903902G>C , CM000663.2:g.173903902G>C	GRCh38
NC_000001.10:g.173873040G>C , CM000663.1:g.173873040G>C	GRCh37
NC_000001.9:g.172139663G>C	NCBI36
NG_012462.1:g.18477C>G , LRG_577:g.18477C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.1382C>G MANE Select	ENSP00000356671.3:p.Pro461Arg
ENST00000367698.3:c.1382C>G	ENSP00000356671.3:p.Pro461Arg
ENST00000617423.4:c.767C>G	ENSP00000478688.1:p.Pro256Arg
NM_000488.3:c.1382C>G , LRG_577t1:c.1382C>G	NP_000479.1:p.Pro461Arg
XM_005245198.2:c.1238C>G	XP_005245255.1:p.Pro413Arg
NM_001365052.1:c.1238C>G	NP_001351981.1:p.Pro413Arg
NM_000488.4:c.1382C>G MANE Select	NP_000479.1:p.Pro461Arg
NM_001365052.2:c.1238C>G	NP_001351981.1:p.Pro413Arg
NM_001386302.1:c.1505C>G	NP_001373231.1:p.Pro502Arg
NM_001386303.1:c.1463C>G	NP_001373232.1:p.Pro488Arg
NM_001386304.1:c.1361C>G	NP_001373233.1:p.Pro454Arg
NM_001386305.1:c.1325C>G	NP_001373234.1:p.Pro442Arg
NM_001386306.1:c.1166C>G	NP_001373235.1:p.Pro389Arg