Canonical Allele Identifier: CA1607966653

Gene: F13A1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.6167508G= , CM000668.2:g.6167508G=	GRCh38
NC_000006.11:g.6167741G= , CM000668.1:g.6167741G=	GRCh37
NC_000006.10:g.6112740G=	NCBI36
NG_008107.1:g.158184C= , LRG_549:g.158184C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000264870.8:c.1858C= MANE Select	ENSP00000264870.3:p.Leu620=
ENST00000264870.7:c.1858C=	ENSP00000264870.3:p.Leu620=
NM_000129.3:c.1858C= , LRG_549t1:c.1858C=	NP_000120.2:p.Leu620=
XM_006715010.2:c.1858C=	XP_006715073.1:p.Leu620=
XM_011514342.1:c.2020C=	XP_011512644.1:p.Leu674=
NM_000129.4:c.1858C= MANE Select	NP_000120.2:p.Leu620=