Canonical Allele Identifier: CA2585300341

Gene: B9D2 TMEM91

Linked Data

• gnomAD v4: 19-41363976-TAGG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41363979_41363981del , CM000681.2:g.41363979_41363981del	GRCh38
NC_000019.9:g.41869884_41869886del , CM000681.1:g.41869884_41869886del	GRCh37
NC_000019.8:g.46561724_46561726del	NCBI36
NG_013091.1:g.5195_5197del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000243578.8:c.-26_-24del (B9D2) MANE Select	ENSP00000243578.2:n.-26_-24del
ENST00000243578.7:c.-26_-24del (B9D2)	ENSP00000243578.2:n.-26_-24del
ENST00000539627.5:c.-30+12777_-30+12779del (TMEM91)	ENSP00000441900.1:n.-30+12777_-30+12779del
ENST00000594416.1:c.-26_-24del (B9D2)	ENSP00000469666.1:n.-26_-24del
ENST00000601597.1:n.114_116del (B9D2)
ENST00000604123.5:c.142+9664_142+9666del (TMEM91)	ENSP00000474871.1:n.142+9664_142+9666del
ENST00000604424.1:n.350+12777_350+12779del
NM_001098825.1:c.-146_-144del (TMEM91)	NP_001092295.1:n.-146_-144del
NM_030578.3:c.-26_-24del (B9D2)	NP_085055.2:n.-26_-24del
XM_006723405.1:c.-26_-24del (B9D2)	XP_006723468.1:n.-26_-24del
XM_011527350.1:c.-93_-91del (B9D2)	XP_011525652.1:n.-93_-91del
XM_011527350.2:c.-93_-91del (B9D2)	XP_011525652.1:n.-93_-91del
NM_030578.4:c.-26_-24del (B9D2) MANE Select	NP_085055.2:n.-26_-24del
NM_001369864.1:c.-403_-401del (TMEM91)	NP_001356793.1:n.-403_-401del
NM_001098825.2:c.-146_-144del (TMEM91)	NP_001092295.1:n.-146_-144del