Canonical Allele Identifier: CA2585300339

Gene: B9D2 TMEM91

Linked Data

• gnomAD v4: 19-41363974-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41363974G>A , CM000681.2:g.41363974G>A	GRCh38
NC_000019.9:g.41869879G>A , CM000681.1:g.41869879G>A	GRCh37
NC_000019.8:g.46561719G>A	NCBI36
NG_013091.1:g.5200C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000243578.8:c.-21C>T (B9D2) MANE Select	ENSP00000243578.2:n.-21C>T
ENST00000243578.7:c.-21C>T (B9D2)	ENSP00000243578.2:n.-21C>T
ENST00000539627.5:c.-30+12772G>A (TMEM91)	ENSP00000441900.1:n.-30+12772G>A
ENST00000594416.1:c.-21C>T (B9D2)	ENSP00000469666.1:n.-21C>T
ENST00000601597.1:n.119C>T (B9D2)
ENST00000604123.5:c.142+9659G>A (TMEM91)	ENSP00000474871.1:n.142+9659G>A
ENST00000604424.1:n.350+12772G>A
NM_001098825.1:c.-151G>A (TMEM91)	NP_001092295.1:n.-151G>A
NM_030578.3:c.-21C>T (B9D2)	NP_085055.2:n.-21C>T
XM_006723405.1:c.-21C>T (B9D2)	XP_006723468.1:n.-21C>T
XM_011527350.1:c.-88C>T (B9D2)	XP_011525652.1:n.-88C>T
XM_011527350.2:c.-88C>T (B9D2)	XP_011525652.1:n.-88C>T
NM_030578.4:c.-21C>T (B9D2) MANE Select	NP_085055.2:n.-21C>T
NM_001369864.1:c.-408G>A (TMEM91)	NP_001356793.1:n.-408G>A
NM_001098825.2:c.-151G>A (TMEM91)	NP_001092295.1:n.-151G>A