Canonical Allele Identifier: CA2340155892

Gene: BAX

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48955313T= , CM000681.2:g.48955313T=	GRCh38
NC_000019.9:g.49458570T= , CM000681.1:g.49458570T=	GRCh37
NC_000019.8:g.54150382T=	NCBI36
NG_012191.1:g.5454T=

Transcript Alleles

HGVS	Amino-acid Change
NM_138761.4:c.35-235T= MANE Select	NP_620116.1:n.35-235T=
ENST00000345358.12:c.35-235T= MANE Select	ENSP00000263262.9:n.35-235T=
NM_001291428.1:c.35-235T=	NP_001278357.1:n.35-235T=
NM_001291428.2:c.35-235T=	NP_001278357.1:n.35-235T=
NM_001291429.1:c.-26+351T=	NP_001278358.1:n.-26+351T=
NM_001291429.2:c.-26+351T=	NP_001278358.1:n.-26+351T=
NM_001291430.1:c.-2+351T=	NP_001278359.1:n.-2+351T=
NM_001291430.2:c.-2+351T=	NP_001278359.1:n.-2+351T=
NM_001291431.1:c.-2+351T=	NP_001278360.1:n.-2+351T=
NM_001291431.2:c.-2+351T=	NP_001278360.1:n.-2+351T=
NM_004324.3:c.35-235T=	NP_004315.1:n.35-235T=
NM_004324.4:c.35-235T=	NP_004315.1:n.35-235T=
NM_138761.3:c.35-235T=	NP_620116.1:n.35-235T=
NM_138763.3:c.35-235T=	NP_620118.1:n.35-235T=
NM_138763.4:c.35-235T=	NP_620118.1:n.35-235T=
NM_138764.4:c.35-235T=	NP_620119.2:n.35-235T=
NM_138764.5:c.35-235T=	NP_620119.2:n.35-235T=
NR_027882.1:n.104-235T=
NR_027882.2:n.89-235T=
ENST00000293288.12:c.35-235T=	ENSP00000293288.8:n.35-235T=
ENST00000345358.11:c.35-235T=	ENSP00000263262.9:n.35-235T=
ENST00000354470.7:c.35-235T=	ENSP00000346461.3:n.35-235T=
ENST00000356483.8:c.35-235T=	ENSP00000348871.4:n.35-235T=
ENST00000391871.4:c.36+349T=	ENSP00000375744.4:n.36+349T=
ENST00000415969.6:c.35-235T=	ENSP00000389971.2:n.35-235T=
ENST00000502487.5:n.499T=
ENST00000506183.5:c.34+351T=
ENST00000513545.5:n.67-235T=
ENST00000515540.5:c.34+351T=	ENSP00000426328.1:n.34+351T=
ENST00000539787.2:c.-2+351T=	ENSP00000441413.2:n.-2+351T=
XM_006723314.2:c.-26+351T=	XP_006723377.1:n.-26+351T=
XM_011527191.1:c.-26+351T=	XP_011525493.1:n.-26+351T=
XM_017027077.1:c.-23-235T=	XP_016882566.1:n.-23-235T=