Canonical Allele Identifier: CA2206128091
Gene: TMEM186 HGNC NCBI
PMM2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.8797642A= , CM000678.2:g.8797642A= GRCh38
NC_000016.9:g.8891499A= , CM000678.1:g.8891499A= GRCh37
NC_000016.8:g.8799000A= NCBI36
NG_009209.1:g.4830A=
NG_033146.1:g.5007T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000333050.6:c.-28T= (TMEM186) ENSP00000331640.6:n.-28T=
ENST00000564869.1:n.1T= (TMEM186)
ENST00000566983.5:c.-15-4157A= (PMM2) ENSP00000457956.1:n.-15-4157A=
NM_015421.3:c.-28T= (TMEM186) NP_056236.2:n.-28T=