Canonical Allele Identifier: CA2336431359

Gene: B9D2 TMEM91

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41363996A= , CM000681.2:g.41363996A=	GRCh38
NC_000019.9:g.41869901A= , CM000681.1:g.41869901A=	GRCh37
NC_000019.8:g.46561741A=	NCBI36
NG_013091.1:g.5178T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000243578.8:c.-43T= (B9D2) MANE Select	ENSP00000243578.2:n.-43T=
ENST00000243578.7:c.-43T= (B9D2)	ENSP00000243578.2:n.-43T=
ENST00000539627.5:c.-30+12794A= (TMEM91)	ENSP00000441900.1:n.-30+12794A=
ENST00000594416.1:c.-43T= (B9D2)	ENSP00000469666.1:n.-43T=
ENST00000601597.1:n.97T= (B9D2)
ENST00000604123.5:c.142+9681A= (TMEM91)	ENSP00000474871.1:n.142+9681A=
ENST00000604424.1:n.350+12794A=
NM_001098825.1:c.-129A= (TMEM91)	NP_001092295.1:n.-129A=
NM_030578.3:c.-43T= (B9D2)	NP_085055.2:n.-43T=
XM_006723405.1:c.-43T= (B9D2)	XP_006723468.1:n.-43T=
XM_011527350.1:c.-110T= (B9D2)	XP_011525652.1:n.-110T=
XM_011527350.2:c.-110T= (B9D2)	XP_011525652.1:n.-110T=
NM_030578.4:c.-43T= (B9D2) MANE Select	NP_085055.2:n.-43T=
NM_001369864.1:c.-386A= (TMEM91)	NP_001356793.1:n.-386A=
NM_001098825.2:c.-129A= (TMEM91)	NP_001092295.1:n.-129A=