Canonical Allele Identifier: CA1607949680

Gene: F13A1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.6145342G= , CM000668.2:g.6145342G=	GRCh38
NC_000006.11:g.6145575G= , CM000668.1:g.6145575G=	GRCh37
NC_000006.10:g.6090574G=	NCBI36
NG_008107.1:g.180350C= , LRG_549:g.180350C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264870.8:c.*277C= MANE Select	ENSP00000264870.3:n.*277C=
ENST00000264870.7:c.*277C=	ENSP00000264870.3:n.*277C=
NM_000129.3:c.*277C= , LRG_549t1:c.*277C=	NP_000120.2:n.*277C=
XM_006715010.2:c.*277C=	XP_006715073.1:n.*277C=
XM_011514342.1:c.*277C=	XP_011512644.1:n.*277C=
NM_000129.4:c.*277C= MANE Select	NP_000120.2:n.*277C=