Canonical Allele Identifier: CA1604287

Gene: BIRC6

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32491450T>G , CM000664.2:g.32491450T>G	GRCh38
NC_000002.11:g.32716517T>G , CM000664.1:g.32716517T>G	GRCh37
NC_000002.10:g.32570021T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700518.1:c.8181T>G	ENSP00000515025.1:p.Thr2727=
ENST00000700519.1:c.8172T>G	ENSP00000515026.1:p.Thr2724=
ENST00000421745.7:c.8232T>G MANE Select	ENSP00000393596.2:p.Thr2744=
ENST00000648282.1:c.8018T>G
ENST00000421745.6:c.8232T>G	ENSP00000393596.2:p.Thr2744=
NM_016252.3:c.8232T>G	NP_057336.3:p.Thr2744=
XM_005264449.3:c.8313T>G	XP_005264506.2:p.Thr2771=
XM_005264450.3:c.8301T>G	XP_005264507.2:p.Thr2767=
XM_005264451.3:c.8286T>G	XP_005264508.2:p.Thr2762=
XM_005264452.3:c.8271T>G	XP_005264509.2:p.Thr2757=
XM_005264453.3:c.8244T>G	XP_005264510.2:p.Thr2748=
XM_005264454.3:c.8313T>G	XP_005264511.2:p.Thr2771=
XM_005264455.3:c.8181T>G	XP_005264512.2:p.Thr2727=
XM_006712054.2:c.8295T>G	XP_006712117.1:p.Thr2765=
XM_006712055.2:c.8313T>G	XP_006712118.1:p.Thr2771=
XM_006712056.2:c.8214T>G	XP_006712119.1:p.Thr2738=
XM_006712057.2:c.8097T>G	XP_006712120.1:p.Thr2699=
XM_011533003.1:c.7998T>G	XP_011531305.1:p.Thr2666=
XM_011533004.1:c.8313T>G	XP_011531306.1:p.Thr2771=
XM_011533005.1:c.8313T>G	XP_011531307.1:p.Thr2771=
XR_244950.3:n.8343T>G
XM_005264449.4:c.8313T>G	XP_005264506.2:p.Thr2771=
XM_005264450.4:c.8301T>G	XP_005264507.2:p.Thr2767=
XM_005264451.4:c.8286T>G	XP_005264508.2:p.Thr2762=
XM_005264452.4:c.8271T>G	XP_005264509.2:p.Thr2757=
XM_005264453.4:c.8244T>G	XP_005264510.2:p.Thr2748=
XM_005264454.5:c.8313T>G	XP_005264511.2:p.Thr2771=
XM_005264455.4:c.8181T>G	XP_005264512.2:p.Thr2727=
XM_006712054.3:c.8295T>G	XP_006712117.1:p.Thr2765=
XM_006712055.3:c.8313T>G	XP_006712118.1:p.Thr2771=
XM_006712056.3:c.8214T>G	XP_006712119.1:p.Thr2738=
XM_011533003.2:c.7998T>G	XP_011531305.1:p.Thr2666=
XM_011533005.2:c.8313T>G	XP_011531307.1:p.Thr2771=
XM_017004556.1:c.8295T>G	XP_016860045.1:p.Thr2765=
XM_017004557.1:c.8202T>G	XP_016860046.1:p.Thr2734=
XM_017004558.1:c.8172T>G	XP_016860047.1:p.Thr2724=
XM_017004559.1:c.8313T>G	XP_016860048.1:p.Thr2771=
XM_017004560.1:c.8295T>G	XP_016860049.1:p.Thr2765=
XR_001738858.2:n.8568T>G
XR_244950.4:n.8568T>G
NM_001378125.1:c.8229T>G	NP_001365054.1:p.Thr2743=
NM_016252.4:c.8232T>G MANE Select	NP_057336.3:p.Thr2744=