Canonical Allele Identifier: CA1607987864

Gene: F13A1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.6224777A= , CM000668.2:g.6224777A=	GRCh38
NC_000006.11:g.6225010A= , CM000668.1:g.6225010A=	GRCh37
NC_000006.10:g.6170009A=	NCBI36
NG_008107.1:g.100915T= , LRG_549:g.100915T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000264870.8:c.882T= MANE Select	ENSP00000264870.3:p.Thr294=
ENST00000264870.7:c.882T=	ENSP00000264870.3:p.Thr294=
ENST00000445223.1:c.32T=
NM_000129.3:c.882T= , LRG_549t1:c.882T=	NP_000120.2:p.Thr294=
XM_006715010.2:c.882T=	XP_006715073.1:p.Thr294=
XM_011514342.1:c.1044T=	XP_011512644.1:p.Thr348=
NM_000129.4:c.882T= MANE Select	NP_000120.2:p.Thr294=