Canonical Allele Identifier: CA2336431202

Gene: B9D2 TMEM91

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41363797C= , CM000681.2:g.41363797C=	GRCh38
NC_000019.9:g.41869702C= , CM000681.1:g.41869702C=	GRCh37
NC_000019.8:g.46561542C=	NCBI36
NG_013091.1:g.5377G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000243578.8:c.-5+161G= (B9D2) MANE Select	ENSP00000243578.2:n.-5+161G=
ENST00000675972.1:c.-38G= (B9D2)	ENSP00000501911.1:n.-38G=
ENST00000243578.7:c.-5+161G= (B9D2)	ENSP00000243578.2:n.-5+161G=
ENST00000539627.5:c.-30+12595C= (TMEM91)	ENSP00000441900.1:n.-30+12595C=
ENST00000594416.1:c.-5+161G= (B9D2)	ENSP00000469666.1:n.-5+161G=
ENST00000601597.1:n.135+161G= (B9D2)
ENST00000604123.5:c.142+9482C= (TMEM91)	ENSP00000474871.1:n.142+9482C=
ENST00000604424.1:n.350+12595C=
NM_030578.3:c.-5+161G= (B9D2)	NP_085055.2:n.-5+161G=
XM_006723405.1:c.-5+161G= (B9D2)	XP_006723468.1:n.-5+161G=
XM_011527349.1:c.-38G= (B9D2)	XP_011525651.1:n.-38G=
XM_011527350.1:c.-72+161G= (B9D2)	XP_011525652.1:n.-72+161G=
XM_011527349.2:c.-38G= (B9D2)	XP_011525651.1:n.-38G=
XM_011527350.2:c.-72+161G= (B9D2)	XP_011525652.1:n.-72+161G=
NM_030578.4:c.-5+161G= (B9D2) MANE Select	NP_085055.2:n.-5+161G=