Canonical Allele Identifier: CA1607993206

Gene: F13A1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.6286110G= , CM000668.2:g.6286110G=	GRCh38
NC_000006.11:g.6286343G= , CM000668.1:g.6286343G=	GRCh37
NC_000006.10:g.6231342G=	NCBI36
NG_008107.1:g.39582C= , LRG_549:g.39582C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000264870.8:c.319+19241C= MANE Select	ENSP00000264870.3:n.319+19241C=
ENST00000264870.7:c.319+19241C=	ENSP00000264870.3:n.319+19241C=
ENST00000414279.5:c.319+19241C=	ENSP00000413334.1:n.319+19241C=
ENST00000431222.6:c.481+19241C=	ENSP00000416295.2:n.481+19241C=
ENST00000479211.1:n.304+19241C=
NM_000129.3:c.319+19241C= , LRG_549t1:c.319+19241C=	NP_000120.2:n.319+19241C=
XM_006715010.2:c.319+19241C=	XP_006715073.1:n.319+19241C=
XM_011514342.1:c.481+19241C=	XP_011512644.1:n.481+19241C=
NM_000129.4:c.319+19241C= MANE Select	NP_000120.2:n.319+19241C=