Canonical Allele Identifier: CA918162686

Gene: TMEM176A

Linked Data

• dbSNP Id: rs1563052386

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150804274_150804275del , CM000669.2:g.150804274_150804275del	GRCh38
NC_000007.13:g.150501362_150501363del , CM000669.1:g.150501362_150501363del	GRCh37
NC_000007.12:g.150132295_150132296del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000004103.8:c.556-88_556-87del MANE Select	ENSP00000004103.3:n.556-88_556-87del
ENST00000468689.2:c.379-88_379-87del	ENSP00000420081.2:n.379-88_379-87del
ENST00000004103.7:c.556-88_556-87del	ENSP00000004103.3:n.556-88_556-87del
ENST00000461345.5:c.379-88_379-87del	ENSP00000420818.1:n.379-88_379-87del
ENST00000462826.1:n.1777+442_1777+443del
ENST00000474166.1:n.215-88_215-87del
ENST00000475007.5:n.452-88_452-87del
ENST00000475536.5:c.412-88_412-87del	ENSP00000417834.1:n.412-88_412-87del
ENST00000481305.1:n.366+442_366+443del
ENST00000484928.5:c.556-88_556-87del	ENSP00000417626.1:n.556-88_556-87del
ENST00000494349.5:n.1102-88_1102-87del
NM_018487.2:c.556-88_556-87del	NP_060957.2:n.556-88_556-87del
XM_011516376.1:c.607-88_607-87del	XP_011514678.1:n.607-88_607-87del
XM_011516377.1:c.607-88_607-87del	XP_011514679.1:n.607-88_607-87del
XM_011516378.1:c.606+442_606+443del	XP_011514680.1:n.606+442_606+443del
XM_011516376.3:c.607-88_607-87del	XP_011514678.1:n.607-88_607-87del
XM_011516377.2:c.607-88_607-87del	XP_011514679.1:n.607-88_607-87del
XM_011516378.2:c.606+442_606+443del	XP_011514680.1:n.606+442_606+443del
XM_017012393.1:c.556-88_556-87del	XP_016867882.1:n.556-88_556-87del
XM_024446824.1:c.555+442_555+443del	XP_024302592.1:n.555+442_555+443del
NM_018487.3:c.556-88_556-87del MANE Select	NP_060957.2:n.556-88_556-87del