Canonical Allele Identifier: CA1207937836

Gene: SERPINC1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173911938A= , CM000663.2:g.173911938A=	GRCh38
NC_000001.10:g.173881076A= , CM000663.1:g.173881076A=	GRCh37
NC_000001.9:g.172147699A=	NCBI36
NG_012462.1:g.10441T= , LRG_577:g.10441T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000367698.4:c.485T= MANE Select	ENSP00000356671.3:p.Leu162=
ENST00000367698.3:c.485T=	ENSP00000356671.3:p.Leu162=
ENST00000487183.1:n.190T=
ENST00000617423.4:c.485T=	ENSP00000478688.1:p.Leu162=
NM_000488.3:c.485T= , LRG_577t1:c.485T=	NP_000479.1:p.Leu162=
XM_005245198.2:c.341T=	XP_005245255.1:p.Leu114=
NM_001365052.1:c.341T=	NP_001351981.1:p.Leu114=
NM_000488.4:c.485T= MANE Select	NP_000479.1:p.Leu162=
NM_001365052.2:c.341T=	NP_001351981.1:p.Leu114=
NM_001386302.1:c.485T=	NP_001373231.1:p.Leu162=
NM_001386303.1:c.566T=	NP_001373232.1:p.Leu189=
NM_001386304.1:c.485T=	NP_001373233.1:p.Leu162=
NM_001386305.1:c.485T=	NP_001373234.1:p.Leu162=
NM_001386306.1:c.409-1047T=	NP_001373235.1:n.409-1047T=