Canonical Allele Identifier: CA406006745

Gene: TMEM91

Linked Data

• gnomAD v4: 19-41354211-G-T
• MyVariant Identifiers: chr19:g.41860116G>T (hg19) ; chr19:g.41354211G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41354211G>T , CM000681.2:g.41354211G>T	GRCh38
NC_000019.9:g.41860116G>T , CM000681.1:g.41860116G>T	GRCh37
NC_000019.8:g.46551956G>T	NCBI36
NG_013091.1:g.14963C>A
NG_013364.1:g.4716C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539627.5:c.-30+3009G>T	ENSP00000441900.1:n.-30+3009G>T
ENST00000604123.5:c.38G>T	ENSP00000474871.1:p.Arg13Ile
ENST00000604424.1:n.350+3009G>T