Canonical Allele Identifier: CA1207937039

Gene: SERPINC1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173909889G= , CM000663.2:g.173909889G=	GRCh38
NC_000001.10:g.173879027G= , CM000663.1:g.173879027G=	GRCh37
NC_000001.9:g.172145650G=	NCBI36
NG_012462.1:g.12490C= , LRG_577:g.12490C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.816C= MANE Select	ENSP00000356671.3:p.Tyr272=
ENST00000367698.3:c.816C=	ENSP00000356671.3:p.Tyr272=
ENST00000487183.1:n.467C=
ENST00000617423.4:c.559+1975C=	ENSP00000478688.1:n.559+1975C=
NM_000488.3:c.816C= , LRG_577t1:c.816C=	NP_000479.1:p.Tyr272=
XM_005245198.2:c.672C=	XP_005245255.1:p.Tyr224=
NM_001365052.1:c.672C=	NP_001351981.1:p.Tyr224=
NM_000488.4:c.816C= MANE Select	NP_000479.1:p.Tyr272=
NM_001365052.2:c.672C=	NP_001351981.1:p.Tyr224=
NM_001386302.1:c.939C=	NP_001373231.1:p.Tyr313=
NM_001386303.1:c.897C=	NP_001373232.1:p.Tyr299=
NM_001386304.1:c.795C=	NP_001373233.1:p.Tyr265=
NM_001386305.1:c.763-4C=	NP_001373234.1:n.763-4C=
NM_001386306.1:c.600C=	NP_001373235.1:p.Tyr200=