Canonical Allele Identifier: CA2336426996
Gene: TMEM91 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41354309A= , CM000681.2:g.41354309A= GRCh38
NC_000019.9:g.41860214A= , CM000681.1:g.41860214A= GRCh37
NC_000019.8:g.46552054A= NCBI36
NG_013091.1:g.14865T=
NG_013364.1:g.4618T=

Transcript Alleles

HGVS Amino-acid change
ENST00000539627.5:c.-30+3107A= ENSP00000441900.1:n.-30+3107A=
ENST00000604123.5:c.136A= ENSP00000474871.1:p.Lys46=
ENST00000604424.1:n.350+3107A=