Canonical Allele Identifier: CA1607987865

Gene: F13A1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.6224786C= , CM000668.2:g.6224786C=	GRCh38
NC_000006.11:g.6225019C= , CM000668.1:g.6225019C=	GRCh37
NC_000006.10:g.6170018C=	NCBI36
NG_008107.1:g.100906G= , LRG_549:g.100906G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000264870.8:c.873G= MANE Select	ENSP00000264870.3:p.Ser291=
ENST00000264870.7:c.873G=	ENSP00000264870.3:p.Ser291=
ENST00000445223.1:c.23G=
NM_000129.3:c.873G= , LRG_549t1:c.873G=	NP_000120.2:p.Ser291=
XM_006715010.2:c.873G=	XP_006715073.1:p.Ser291=
XM_011514342.1:c.1035G=	XP_011512644.1:p.Ser345=
NM_000129.4:c.873G= MANE Select	NP_000120.2:p.Ser291=