Canonical Allele Identifier: CA1607987880

Gene: F13A1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.6224811A= , CM000668.2:g.6224811A=	GRCh38
NC_000006.11:g.6225044A= , CM000668.1:g.6225044A=	GRCh37
NC_000006.10:g.6170043A=	NCBI36
NG_008107.1:g.100881T= , LRG_549:g.100881T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000264870.8:c.848T= MANE Select	ENSP00000264870.3:p.Ile283=
ENST00000264870.7:c.848T=	ENSP00000264870.3:p.Ile283=
NM_000129.3:c.848T= , LRG_549t1:c.848T=	NP_000120.2:p.Ile283=
XM_006715010.2:c.848T=	XP_006715073.1:p.Ile283=
XM_011514342.1:c.1010T=	XP_011512644.1:p.Ile337=
NM_000129.4:c.848T= MANE Select	NP_000120.2:p.Ile283=