Canonical Allele Identifier: CA1605527

Gene: BIRC6

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32593943G>A , CM000664.2:g.32593943G>A	GRCh38
NC_000002.11:g.32819010G>A , CM000664.1:g.32819010G>A	GRCh37
NC_000002.10:g.32672514G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700518.1:c.13333G>A	ENSP00000515025.1:p.Val4445Ile
ENST00000700519.1:c.13324G>A	ENSP00000515026.1:p.Val4442Ile
ENST00000421745.7:c.13384G>A MANE Select	ENSP00000393596.2:p.Val4462Ile
ENST00000421745.6:c.13384G>A	ENSP00000393596.2:p.Val4462Ile
ENST00000470250.1:n.105G>A
ENST00000471232.5:n.2064G>A
NM_016252.3:c.13384G>A	NP_057336.3:p.Val4462Ile
XM_005264449.3:c.13465G>A	XP_005264506.2:p.Val4489Ile
XM_005264450.3:c.13453G>A	XP_005264507.2:p.Val4485Ile
XM_005264451.3:c.13438G>A	XP_005264508.2:p.Val4480Ile
XM_005264452.3:c.13423G>A	XP_005264509.2:p.Val4475Ile
XM_005264453.3:c.13396G>A	XP_005264510.2:p.Val4466Ile
XM_005264454.3:c.13465G>A	XP_005264511.2:p.Val4489Ile
XM_005264455.3:c.13333G>A	XP_005264512.2:p.Val4445Ile
XM_006712054.2:c.13447G>A	XP_006712117.1:p.Val4483Ile
XM_006712055.2:c.13405G>A	XP_006712118.1:p.Val4469Ile
XM_006712056.2:c.13366G>A	XP_006712119.1:p.Val4456Ile
XM_006712057.2:c.13249G>A	XP_006712120.1:p.Val4417Ile
XM_011533003.1:c.13150G>A	XP_011531305.1:p.Val4384Ile
XM_011533004.1:c.13465G>A	XP_011531306.1:p.Val4489Ile
XR_244950.3:n.13668G>A
XM_005264449.4:c.13465G>A	XP_005264506.2:p.Val4489Ile
XM_005264450.4:c.13453G>A	XP_005264507.2:p.Val4485Ile
XM_005264451.4:c.13438G>A	XP_005264508.2:p.Val4480Ile
XM_005264452.4:c.13423G>A	XP_005264509.2:p.Val4475Ile
XM_005264453.4:c.13396G>A	XP_005264510.2:p.Val4466Ile
XM_005264454.5:c.13465G>A	XP_005264511.2:p.Val4489Ile
XM_005264455.4:c.13333G>A	XP_005264512.2:p.Val4445Ile
XM_006712054.3:c.13447G>A	XP_006712117.1:p.Val4483Ile
XM_006712055.3:c.13405G>A	XP_006712118.1:p.Val4469Ile
XM_006712056.3:c.13366G>A	XP_006712119.1:p.Val4456Ile
XM_011533003.2:c.13150G>A	XP_011531305.1:p.Val4384Ile
XM_017004556.1:c.13387G>A	XP_016860045.1:p.Val4463Ile
XM_017004557.1:c.13354G>A	XP_016860046.1:p.Val4452Ile
XM_017004558.1:c.13324G>A	XP_016860047.1:p.Val4442Ile
XM_017004559.1:c.13465G>A	XP_016860048.1:p.Val4489Ile
XR_001738858.2:n.13893G>A
XR_244950.4:n.13893G>A
NM_001378125.1:c.13381G>A	NP_001365054.1:p.Val4461Ile
NM_016252.4:c.13384G>A MANE Select	NP_057336.3:p.Val4462Ile