Canonical Allele Identifier: CA1607949693

Gene: F13A1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.6145367G= , CM000668.2:g.6145367G=	GRCh38
NC_000006.11:g.6145600G= , CM000668.1:g.6145600G=	GRCh37
NC_000006.10:g.6090599G=	NCBI36
NG_008107.1:g.180325C= , LRG_549:g.180325C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264870.8:c.*252C= MANE Select	ENSP00000264870.3:n.*252C=
ENST00000264870.7:c.*252C=	ENSP00000264870.3:n.*252C=
NM_000129.3:c.*252C= , LRG_549t1:c.*252C=	NP_000120.2:n.*252C=
XM_006715010.2:c.*252C=	XP_006715073.1:n.*252C=
XM_011514342.1:c.*252C=	XP_011512644.1:n.*252C=
NM_000129.4:c.*252C= MANE Select	NP_000120.2:n.*252C=