Canonical Allele Identifier: CA1607993191

Gene: F13A1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.6286080A= , CM000668.2:g.6286080A=	GRCh38
NC_000006.11:g.6286313A= , CM000668.1:g.6286313A=	GRCh37
NC_000006.10:g.6231312A=	NCBI36
NG_008107.1:g.39612T= , LRG_549:g.39612T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000264870.8:c.320-19271T= MANE Select	ENSP00000264870.3:n.320-19271T=
ENST00000264870.7:c.320-19271T=	ENSP00000264870.3:n.320-19271T=
ENST00000414279.5:c.320-19271T=	ENSP00000413334.1:n.320-19271T=
ENST00000431222.6:c.482-19271T=	ENSP00000416295.2:n.482-19271T=
ENST00000479211.1:n.305-19271T=
NM_000129.3:c.320-19271T= , LRG_549t1:c.320-19271T=	NP_000120.2:n.320-19271T=
XM_006715010.2:c.320-19271T=	XP_006715073.1:n.320-19271T=
XM_011514342.1:c.482-19271T=	XP_011512644.1:n.482-19271T=
NM_000129.4:c.320-19271T= MANE Select	NP_000120.2:n.320-19271T=