Canonical Allele Identifier: CA458642974

Gene: TMEM176A

Linked Data

• MyVariant Identifiers: chr7:g.150501551A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150804463A>C , CM000669.2:g.150804463A>C	GRCh38
NC_000007.13:g.150501551A>C , CM000669.1:g.150501551A>C	GRCh37
NC_000007.12:g.150132484A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000004103.8:c.657A>C MANE Select	ENSP00000004103.3:p.Pro219=
ENST00000468689.2:c.480A>C	ENSP00000420081.2:p.Pro160=
ENST00000004103.7:c.657A>C	ENSP00000004103.3:p.Pro219=
ENST00000461345.5:c.480A>C	ENSP00000420818.1:p.Pro160=
ENST00000462826.1:n.1778-364A>C
ENST00000474166.1:n.316A>C
ENST00000475007.5:n.553A>C
ENST00000475536.5:c.513A>C	ENSP00000417834.1:p.Pro171=
ENST00000481305.1:n.367-364A>C
ENST00000484928.5:c.657A>C	ENSP00000417626.1:p.Pro219=
ENST00000494349.5:n.1203A>C
NM_018487.2:c.657A>C	NP_060957.2:p.Pro219=
XM_011516376.1:c.708A>C	XP_011514678.1:p.Pro236=
XM_011516377.1:c.708A>C	XP_011514679.1:p.Pro236=
XM_011516378.1:c.607-364A>C	XP_011514680.1:n.607-364A>C
XM_011516376.3:c.708A>C	XP_011514678.1:p.Pro236=
XM_011516377.2:c.708A>C	XP_011514679.1:p.Pro236=
XM_011516378.2:c.607-364A>C	XP_011514680.1:n.607-364A>C
XM_017012393.1:c.657A>C	XP_016867882.1:p.Pro219=
XM_024446824.1:c.556-364A>C	XP_024302592.1:n.556-364A>C
NM_018487.3:c.657A>C MANE Select	NP_060957.2:p.Pro219=