Canonical Allele Identifier: CA2206128089

Gene: TMEM186 PMM2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.8797637A= , CM000678.2:g.8797637A=	GRCh38
NC_000016.9:g.8891494A= , CM000678.1:g.8891494A=	GRCh37
NC_000016.8:g.8798995A=	NCBI36
NG_009209.1:g.4825A=
NG_033146.1:g.5012T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333050.7:c.-23T= (TMEM186) MANE Select	ENSP00000331640.6:n.-23T=
ENST00000333050.6:c.-23T= (TMEM186)	ENSP00000331640.6:n.-23T=
ENST00000564869.1:n.6T= (TMEM186)
ENST00000566983.5:c.-15-4162A= (PMM2)	ENSP00000457956.1:n.-15-4162A=
NM_015421.3:c.-23T= (TMEM186)	NP_056236.2:n.-23T=
NM_015421.4:c.-23T= (TMEM186) MANE Select	NP_056236.2:n.-23T=