Canonical Allele Identifier: CA9580702

Gene: BCL2L12

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49665980G>C , CM000681.2:g.49665980G>C	GRCh38
NC_000019.9:g.50169237G>C , CM000681.1:g.50169237G>C	GRCh37
NC_000019.8:g.54861049G>C	NCBI36
NG_031810.1:g.4896C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_138639.2:c.-96G>C MANE Select	NP_619580.2:n.-96G>C
ENST00000246784.8:c.-96G>C MANE Select	ENSP00000246784.4:n.-96G>C
NM_001040668.1:c.157G>C	NP_001035758.1:p.Gly53Arg
NM_001040668.2:c.-96G>C	NP_001035758.2:n.-96G>C
NM_001282516.1:c.157G>C	NP_001269445.1:p.Gly53Arg
NM_001282516.2:c.-96G>C	NP_001269445.2:n.-96G>C
NM_001282517.1:c.157G>C	NP_001269446.1:p.Gly53Arg
NM_001282517.2:c.-96G>C	NP_001269446.2:n.-96G>C
NM_001282519.1:c.157G>C	NP_001269448.1:p.Gly53Arg
NM_001282519.2:c.-96G>C	NP_001269448.2:n.-96G>C
NM_001282520.1:c.157G>C	NP_001269449.1:p.Gly53Arg
NM_001282521.1:c.157G>C	NP_001269450.1:p.Gly53Arg
NM_001282521.2:c.-96G>C	NP_001269450.2:n.-96G>C
NM_001385706.1:c.-96G>C	NP_001372635.1:n.-96G>C
NM_138639.1:c.157G>C	NP_619580.1:p.Gly53Arg
NR_104200.1:n.839G>C
NR_104201.1:n.839G>C
NR_104202.1:n.839G>C
NR_104203.1:n.839G>C
NR_104204.1:n.839G>C
NR_104205.1:n.839G>C
ENST00000246785.7:c.157G>C	ENSP00000246785.2:p.Gly53Arg
ENST00000441864.6:c.157G>C	ENSP00000393803.1:p.Gly53Arg
ENST00000594157.5:c.-96G>C	ENSP00000469216.2:n.-96G>C
ENST00000598979.5:c.-96G>C	ENSP00000471919.2:n.-96G>C
ENST00000611631.4:c.157G>C	ENSP00000478415.1:p.Gly53Arg
ENST00000614495.4:c.157G>C	ENSP00000482154.1:p.Gly53Arg
ENST00000616144.4:c.157G>C	ENSP00000482218.1:p.Gly53Arg
ENST00000619007.4:c.157G>C	ENSP00000483272.1:p.Gly53Arg
ENST00000698553.1:c.-713G>C	ENSP00000513795.1:n.-713G>C
ENST00000698554.1:c.-713G>C	ENSP00000513796.1:n.-713G>C
ENST00000698555.1:c.-713G>C	ENSP00000513797.1:n.-713G>C
ENST00000698556.1:c.-713G>C	ENSP00000513798.1:n.-713G>C
ENST00000698557.1:c.-713G>C	ENSP00000513799.1:n.-713G>C
ENST00000698558.1:c.-713G>C	ENSP00000513800.1:n.-713G>C
ENST00000698559.1:c.-713G>C	ENSP00000513801.1:n.-713G>C
ENST00000698560.1:c.-713G>C	ENSP00000513802.1:n.-713G>C
ENST00000698561.1:c.-713G>C	ENSP00000513803.1:n.-713G>C
XM_017027345.2:c.157G>C	XP_016882834.1:p.Gly53Arg
XM_017027346.2:c.157G>C	XP_016882835.1:p.Gly53Arg