Canonical Allele Identifier: CA406006980
Gene: TMEM91 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41354303G>C , CM000681.2:g.41354303G>C GRCh38
NC_000019.9:g.41860208G>C , CM000681.1:g.41860208G>C GRCh37
NC_000019.8:g.46552048G>C NCBI36
NG_013091.1:g.14871C>G
NG_013364.1:g.4624C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000539627.5:c.-30+3101G>C ENSP00000441900.1:n.-30+3101G>C
ENST00000604123.5:c.130G>C ENSP00000474871.1:p.Ala44Pro
ENST00000604424.1:n.350+3101G>C