Canonical Allele Identifier: CA2206128079

Gene: TMEM186 PMM2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.8797625C= , CM000678.2:g.8797625C=	GRCh38
NC_000016.9:g.8891482C= , CM000678.1:g.8891482C=	GRCh37
NC_000016.8:g.8798983C=	NCBI36
NG_009209.1:g.4813C=
NG_033146.1:g.5024G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333050.7:c.-11G= (TMEM186) MANE Select	ENSP00000331640.6:n.-11G=
ENST00000333050.6:c.-11G= (TMEM186)	ENSP00000331640.6:n.-11G=
ENST00000564869.1:n.18G= (TMEM186)
ENST00000566983.5:c.-15-4174C= (PMM2)	ENSP00000457956.1:n.-15-4174C=
NM_015421.3:c.-11G= (TMEM186)	NP_056236.2:n.-11G=
NM_015421.4:c.-11G= (TMEM186) MANE Select	NP_056236.2:n.-11G=