Canonical Allele Identifier: CA406007010

Gene: TMEM91

Linked Data

• MyVariant Identifiers: chr19:g.41860220G>A (hg19) ; chr19:g.41354315G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41354315G>A , CM000681.2:g.41354315G>A	GRCh38
NC_000019.9:g.41860220G>A , CM000681.1:g.41860220G>A	GRCh37
NC_000019.8:g.46552060G>A	NCBI36
NG_013091.1:g.14859C>T
NG_013364.1:g.4612C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000539627.5:c.-30+3113G>A	ENSP00000441900.1:n.-30+3113G>A
ENST00000604123.5:c.142G>A	ENSP00000474871.1:p.Gly48Arg
ENST00000604424.1:n.350+3113G>A