Canonical Allele Identifier: CA406006965
Gene: TMEM91 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41354297A>C , CM000681.2:g.41354297A>C GRCh38
NC_000019.9:g.41860202A>C , CM000681.1:g.41860202A>C GRCh37
NC_000019.8:g.46552042A>C NCBI36
NG_013091.1:g.14877T>G
NG_013364.1:g.4630T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000539627.5:c.-30+3095A>C ENSP00000441900.1:n.-30+3095A>C
ENST00000604123.5:c.124A>C ENSP00000474871.1:p.Ser42Arg
ENST00000604424.1:n.350+3095A>C