Canonical Allele Identifier: CA1607949602

Gene: F13A1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.6145141A= , CM000668.2:g.6145141A=	GRCh38
NC_000006.11:g.6145374A= , CM000668.1:g.6145374A=	GRCh37
NC_000006.10:g.6090373A=	NCBI36
NG_008107.1:g.180551T= , LRG_549:g.180551T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264870.8:c.*478T= MANE Select	ENSP00000264870.3:n.*478T=
ENST00000264870.7:c.*478T=	ENSP00000264870.3:n.*478T=
NM_000129.3:c.*478T= , LRG_549t1:c.*478T=	NP_000120.2:n.*478T=
XM_006715010.2:c.*478T=	XP_006715073.1:n.*478T=
XM_011514342.1:c.*478T=	XP_011512644.1:n.*478T=
NM_000129.4:c.*478T= MANE Select	NP_000120.2:n.*478T=