Canonical Allele Identifier: CA406006994

Gene: TMEM91

Linked Data

• gnomAD v4: 19-41354310-A-G
• MyVariant Identifiers: chr19:g.41860215A>G (hg19) ; chr19:g.41354310A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41354310A>G , CM000681.2:g.41354310A>G	GRCh38
NC_000019.9:g.41860215A>G , CM000681.1:g.41860215A>G	GRCh37
NC_000019.8:g.46552055A>G	NCBI36
NG_013091.1:g.14864T>C
NG_013364.1:g.4617T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539627.5:c.-30+3108A>G	ENSP00000441900.1:n.-30+3108A>G
ENST00000604123.5:c.137A>G	ENSP00000474871.1:p.Lys46Arg
ENST00000604424.1:n.350+3108A>G