Canonical Allele Identifier: CA369842976

Gene: TMEM176A

Linked Data

• MyVariant Identifiers: chr7:g.150501469A>C (hg19) ; chr7:g.150804381A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150804381A>C , CM000669.2:g.150804381A>C	GRCh38
NC_000007.13:g.150501469A>C , CM000669.1:g.150501469A>C	GRCh37
NC_000007.12:g.150132402A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000004103.8:c.575A>C MANE Select	ENSP00000004103.3:p.Gln192Pro
ENST00000468689.2:c.398A>C	ENSP00000420081.2:p.Gln133Pro
ENST00000004103.7:c.575A>C	ENSP00000004103.3:p.Gln192Pro
ENST00000461345.5:c.398A>C	ENSP00000420818.1:p.Gln133Pro
ENST00000462826.1:n.1778-446A>C
ENST00000474166.1:n.234A>C
ENST00000475007.5:n.471A>C
ENST00000475536.5:c.431A>C	ENSP00000417834.1:p.Gln144Pro
ENST00000481305.1:n.367-446A>C
ENST00000484928.5:c.575A>C	ENSP00000417626.1:p.Gln192Pro
ENST00000494349.5:n.1121A>C
NM_018487.2:c.575A>C	NP_060957.2:p.Gln192Pro
XM_011516376.1:c.626A>C	XP_011514678.1:p.Gln209Pro
XM_011516377.1:c.626A>C	XP_011514679.1:p.Gln209Pro
XM_011516378.1:c.607-446A>C	XP_011514680.1:n.607-446A>C
XM_011516376.3:c.626A>C	XP_011514678.1:p.Gln209Pro
XM_011516377.2:c.626A>C	XP_011514679.1:p.Gln209Pro
XM_011516378.2:c.607-446A>C	XP_011514680.1:n.607-446A>C
XM_017012393.1:c.575A>C	XP_016867882.1:p.Gln192Pro
XM_024446824.1:c.556-446A>C	XP_024302592.1:n.556-446A>C
NM_018487.3:c.575A>C MANE Select	NP_060957.2:p.Gln192Pro