Canonical Allele Identifier: CA1605528

Gene: BIRC6

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32593957G>A , CM000664.2:g.32593957G>A	GRCh38
NC_000002.11:g.32819024G>A , CM000664.1:g.32819024G>A	GRCh37
NC_000002.10:g.32672528G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700518.1:c.13347G>A	ENSP00000515025.1:p.Ala4449=
ENST00000700519.1:c.13338G>A	ENSP00000515026.1:p.Ala4446=
ENST00000421745.7:c.13398G>A MANE Select	ENSP00000393596.2:p.Ala4466=
ENST00000421745.6:c.13398G>A	ENSP00000393596.2:p.Ala4466=
ENST00000470250.1:n.119G>A
ENST00000471232.5:n.2078G>A
NM_016252.3:c.13398G>A	NP_057336.3:p.Ala4466=
XM_005264449.3:c.13479G>A	XP_005264506.2:p.Ala4493=
XM_005264450.3:c.13467G>A	XP_005264507.2:p.Ala4489=
XM_005264451.3:c.13452G>A	XP_005264508.2:p.Ala4484=
XM_005264452.3:c.13437G>A	XP_005264509.2:p.Ala4479=
XM_005264453.3:c.13410G>A	XP_005264510.2:p.Ala4470=
XM_005264454.3:c.13479G>A	XP_005264511.2:p.Ala4493=
XM_005264455.3:c.13347G>A	XP_005264512.2:p.Ala4449=
XM_006712054.2:c.13461G>A	XP_006712117.1:p.Ala4487=
XM_006712055.2:c.13419G>A	XP_006712118.1:p.Ala4473=
XM_006712056.2:c.13380G>A	XP_006712119.1:p.Ala4460=
XM_006712057.2:c.13263G>A	XP_006712120.1:p.Ala4421=
XM_011533003.1:c.13164G>A	XP_011531305.1:p.Ala4388=
XM_011533004.1:c.13479G>A	XP_011531306.1:p.Ala4493=
XR_244950.3:n.13682G>A
XM_005264449.4:c.13479G>A	XP_005264506.2:p.Ala4493=
XM_005264450.4:c.13467G>A	XP_005264507.2:p.Ala4489=
XM_005264451.4:c.13452G>A	XP_005264508.2:p.Ala4484=
XM_005264452.4:c.13437G>A	XP_005264509.2:p.Ala4479=
XM_005264453.4:c.13410G>A	XP_005264510.2:p.Ala4470=
XM_005264454.5:c.13479G>A	XP_005264511.2:p.Ala4493=
XM_005264455.4:c.13347G>A	XP_005264512.2:p.Ala4449=
XM_006712054.3:c.13461G>A	XP_006712117.1:p.Ala4487=
XM_006712055.3:c.13419G>A	XP_006712118.1:p.Ala4473=
XM_006712056.3:c.13380G>A	XP_006712119.1:p.Ala4460=
XM_011533003.2:c.13164G>A	XP_011531305.1:p.Ala4388=
XM_017004556.1:c.13401G>A	XP_016860045.1:p.Ala4467=
XM_017004557.1:c.13368G>A	XP_016860046.1:p.Ala4456=
XM_017004558.1:c.13338G>A	XP_016860047.1:p.Ala4446=
XM_017004559.1:c.13479G>A	XP_016860048.1:p.Ala4493=
XR_001738858.2:n.13907G>A
XR_244950.4:n.13907G>A
NM_001378125.1:c.13395G>A	NP_001365054.1:p.Ala4465=
NM_016252.4:c.13398G>A MANE Select	NP_057336.3:p.Ala4466=