Canonical Allele Identifier: CA633167812
Gene: TMEM91 HGNC NCBI

Linked Data

dbSNP Id: rs1422997957
gnomAD v2: 19-41860114-GAGAA-G
gnomAD v3: 19-41354209-GAGAA-G
gnomAD v4: 19-41354209-GAGAA-G
MyVariant Identifiers: chr19:g.41860115_41860118del (hg19) chr19:g.41354210_41354213del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41354213_41354216del , CM000681.2:g.41354213_41354216del GRCh38
NC_000019.9:g.41860118_41860121del , CM000681.1:g.41860118_41860121del GRCh37
NC_000019.8:g.46551958_46551961del NCBI36
NG_013091.1:g.14961_14964del
NG_013364.1:g.4714_4717del

Transcript Alleles

HGVS Amino-acid Change
ENST00000539627.5:c.-30+3011_-30+3014del ENSP00000441900.1:n.-30+3011_-30+3014del
ENST00000604123.5:c.40_43del ENSP00000474871.1:p.Lys14GlyfsTer?
ENST00000604424.1:n.350+3011_350+3014del
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