Canonical Allele Identifier: CA2336427559

Gene: B9D2 TMEM91

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41355502A= , CM000681.2:g.41355502A=	GRCh38
NC_000019.9:g.41861407A= , CM000681.1:g.41861407A=	GRCh37
NC_000019.8:g.46553247A=	NCBI36
NG_013091.1:g.13672T=
NG_013364.1:g.3425T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000243578.8:c.215-489T= (B9D2) MANE Select	ENSP00000243578.2:n.215-489T=
ENST00000675972.1:c.215-489T= (B9D2)	ENSP00000501911.1:n.215-489T=
ENST00000243578.7:c.215-489T= (B9D2)	ENSP00000243578.2:n.215-489T=
ENST00000539627.5:c.-30+4300A= (TMEM91)	ENSP00000441900.1:n.-30+4300A=
ENST00000594416.1:c.*61-489T= (B9D2)	ENSP00000469666.1:n.*61-489T=
ENST00000604123.5:c.142+1187A= (TMEM91)	ENSP00000474871.1:n.142+1187A=
ENST00000604424.1:n.350+4300A=
NM_030578.3:c.215-489T= (B9D2)	NP_085055.2:n.215-489T=
XM_006723405.1:c.89-489T= (B9D2)	XP_006723468.1:n.89-489T=
XM_011527349.1:c.215-489T= (B9D2)	XP_011525651.1:n.215-489T=
XM_011527350.1:c.56-489T= (B9D2)	XP_011525652.1:n.56-489T=
XM_011527349.2:c.215-489T= (B9D2)	XP_011525651.1:n.215-489T=
XM_011527350.2:c.56-489T= (B9D2)	XP_011525652.1:n.56-489T=
NM_030578.4:c.215-489T= (B9D2) MANE Select	NP_085055.2:n.215-489T=