Canonical Allele Identifier: CA406006954
Gene: TMEM91 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41354294G>A , CM000681.2:g.41354294G>A GRCh38
NC_000019.9:g.41860199G>A , CM000681.1:g.41860199G>A GRCh37
NC_000019.8:g.46552039G>A NCBI36
NG_013091.1:g.14880C>T
NG_013364.1:g.4633C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000539627.5:c.-30+3092G>A ENSP00000441900.1:n.-30+3092G>A
ENST00000604123.5:c.121G>A ENSP00000474871.1:p.Glu41Lys
ENST00000604424.1:n.350+3092G>A