Canonical Allele Identifier: CA2579062404

Gene: TMEM176A

Linked Data

• gnomAD v4: 7-150804281-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150804281C>A , CM000669.2:g.150804281C>A	GRCh38
NC_000007.13:g.150501369C>A , CM000669.1:g.150501369C>A	GRCh37
NC_000007.12:g.150132302C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000004103.8:c.556-81C>A MANE Select	ENSP00000004103.3:n.556-81C>A
ENST00000468689.2:c.379-81C>A	ENSP00000420081.2:n.379-81C>A
ENST00000004103.7:c.556-81C>A	ENSP00000004103.3:n.556-81C>A
ENST00000461345.5:c.379-81C>A	ENSP00000420818.1:n.379-81C>A
ENST00000462826.1:n.1777+449C>A
ENST00000474166.1:n.215-81C>A
ENST00000475007.5:n.452-81C>A
ENST00000475536.5:c.412-81C>A	ENSP00000417834.1:n.412-81C>A
ENST00000481305.1:n.366+449C>A
ENST00000484928.5:c.556-81C>A	ENSP00000417626.1:n.556-81C>A
ENST00000494349.5:n.1102-81C>A
NM_018487.2:c.556-81C>A	NP_060957.2:n.556-81C>A
XM_011516376.1:c.607-81C>A	XP_011514678.1:n.607-81C>A
XM_011516377.1:c.607-81C>A	XP_011514679.1:n.607-81C>A
XM_011516378.1:c.606+449C>A	XP_011514680.1:n.606+449C>A
XM_011516376.3:c.607-81C>A	XP_011514678.1:n.607-81C>A
XM_011516377.2:c.607-81C>A	XP_011514679.1:n.607-81C>A
XM_011516378.2:c.606+449C>A	XP_011514680.1:n.606+449C>A
XM_017012393.1:c.556-81C>A	XP_016867882.1:n.556-81C>A
XM_024446824.1:c.555+449C>A	XP_024302592.1:n.555+449C>A
NM_018487.3:c.556-81C>A MANE Select	NP_060957.2:n.556-81C>A