Canonical Allele Identifier: CA2336426947
Gene: TMEM91 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41354201G= , CM000681.2:g.41354201G= GRCh38
NC_000019.9:g.41860106G= , CM000681.1:g.41860106G= GRCh37
NC_000019.8:g.46551946G= NCBI36
NG_013091.1:g.14973C=
NG_013364.1:g.4726C=

Transcript Alleles

HGVS Amino-acid change
ENST00000539627.5:c.-30+2999G= ENSP00000441900.1:n.-30+2999G=
ENST00000604123.5:c.28G= ENSP00000474871.1:p.Gly10=
ENST00000604424.1:n.350+2999G=