Canonical Allele Identifier: CA507560788

Gene: B9D2 TMEM91

Linked Data

• MyVariant Identifiers: chr19:g.41869404G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41363499G>T , CM000681.2:g.41363499G>T	GRCh38
NC_000019.9:g.41869404G>T , CM000681.1:g.41869404G>T	GRCh37
NC_000019.8:g.46561244G>T	NCBI36
NG_013091.1:g.5675C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000243578.8:c.21C>A (B9D2) MANE Select	ENSP00000243578.2:p.Ile7=
ENST00000675972.1:c.21C>A (B9D2)	ENSP00000501911.1:p.Ile7=
ENST00000243578.7:c.21C>A (B9D2)	ENSP00000243578.2:p.Ile7=
ENST00000539627.5:c.-30+12297G>T (TMEM91)	ENSP00000441900.1:n.-30+12297G>T
ENST00000594416.1:c.21C>A (B9D2)	ENSP00000469666.1:p.Ile7=
ENST00000601597.1:n.160C>A (B9D2)
ENST00000604123.5:c.142+9184G>T (TMEM91)	ENSP00000474871.1:n.142+9184G>T
ENST00000604424.1:n.350+12297G>T
NM_030578.3:c.21C>A (B9D2)	NP_085055.2:p.Ile7=
XM_006723405.1:c.21C>A (B9D2)	XP_006723468.1:p.Ile7=
XM_011527349.1:c.21C>A (B9D2)	XP_011525651.1:p.Ile7=
XM_011527350.1:c.-72+459C>A (B9D2)	XP_011525652.1:n.-72+459C>A
XM_011527349.2:c.21C>A (B9D2)	XP_011525651.1:p.Ile7=
XM_011527350.2:c.-72+459C>A (B9D2)	XP_011525652.1:n.-72+459C>A
NM_030578.4:c.21C>A (B9D2) MANE Select	NP_085055.2:p.Ile7=