Canonical Allele Identifier: CA13648430

Gene: TAFA2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.61841052C>T , CM000674.2:g.61841052C>T	GRCh38
NC_000012.11:g.62234833C>T , CM000674.1:g.62234833C>T	GRCh37
NC_000012.10:g.60521100C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000416284.8:c.106+26268G>A MANE Select	ENSP00000393987.3:n.106+26268G>A
ENST00000416284.7:c.106+26268G>A	ENSP00000393987.3:n.106+26268G>A
ENST00000548780.1:c.109+26268G>A	ENSP00000449310.1:n.109+26268G>A
ENST00000549379.5:c.106+26268G>A	ENSP00000447584.1:n.106+26268G>A
ENST00000549958.5:c.127+26268G>A	ENSP00000447280.1:n.127+26268G>A
ENST00000551449.1:c.106+26268G>A	ENSP00000449632.1:n.106+26268G>A
ENST00000551619.5:c.106+26268G>A	ENSP00000447305.1:n.106+26268G>A
ENST00000552075.5:c.109+26268G>A	ENSP00000449516.1:n.109+26268G>A
NM_178539.4:c.106+26268G>A	NP_848634.1:n.106+26268G>A
XM_006719370.2:c.106+26268G>A	XP_006719433.1:n.106+26268G>A
XM_011538272.1:c.106+26268G>A	XP_011536574.1:n.106+26268G>A
XM_011538273.1:c.106+26268G>A	XP_011536575.1:n.106+26268G>A
XM_011538274.1:c.106+26268G>A	XP_011536576.1:n.106+26268G>A
XM_011538275.1:c.106+26268G>A	XP_011536577.1:n.106+26268G>A
XM_011538272.2:c.106+26268G>A	XP_011536574.1:n.106+26268G>A
XM_024448962.1:c.253+26268G>A	XP_024304730.1:n.253+26268G>A
XM_024448963.1:c.109+26268G>A	XP_024304731.1:n.109+26268G>A
XM_024448964.1:c.106+26268G>A	XP_024304732.1:n.106+26268G>A
XM_024448965.1:c.106+26268G>A	XP_024304733.1:n.106+26268G>A
XM_024448966.1:c.106+26268G>A	XP_024304734.1:n.106+26268G>A
NM_178539.5:c.106+26268G>A MANE Select	NP_848634.1:n.106+26268G>A