Canonical Allele Identifier: CA1607949831

Gene: F13A1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.6145663A= , CM000668.2:g.6145663A=	GRCh38
NC_000006.11:g.6145896A= , CM000668.1:g.6145896A=	GRCh37
NC_000006.10:g.6090895A=	NCBI36
NG_008107.1:g.180029T= , LRG_549:g.180029T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264870.8:c.2155T= MANE Select	ENSP00000264870.3:p.Tyr719=
ENST00000264870.7:c.2155T=	ENSP00000264870.3:p.Tyr719=
NM_000129.3:c.2155T= , LRG_549t1:c.2155T=	NP_000120.2:p.Tyr719=
XM_006715010.2:c.2155T=	XP_006715073.1:p.Tyr719=
XM_011514342.1:c.2317T=	XP_011512644.1:p.Tyr773=
NM_000129.4:c.2155T= MANE Select	NP_000120.2:p.Tyr719=