Canonical Allele Identifier: CA1603093

Gene: BIRC6

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32433719C>T , CM000664.2:g.32433719C>T	GRCh38
NC_000002.11:g.32658787C>T , CM000664.1:g.32658787C>T	GRCh37
NC_000002.10:g.32512291C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_016252.4:c.3324C>T MANE Select	NP_057336.3:p.Phe1108=
ENST00000421745.7:c.3324C>T MANE Select	ENSP00000393596.2:p.Phe1108=
NM_001378125.1:c.3240C>T	NP_001365054.1:p.Phe1080=
NM_016252.3:c.3324C>T	NP_057336.3:p.Phe1108=
ENST00000421745.6:c.3324C>T	ENSP00000393596.2:p.Phe1108=
ENST00000444173.5:c.72C>T	ENSP00000413090.1:p.Phe24=
ENST00000648282.1:c.3161C>T
ENST00000700518.1:c.3324C>T	ENSP00000515025.1:p.Phe1108=
ENST00000700519.1:c.3324C>T	ENSP00000515026.1:p.Phe1108=
XM_005264449.3:c.3324C>T	XP_005264506.2:p.Phe1108=
XM_005264449.4:c.3324C>T	XP_005264506.2:p.Phe1108=
XM_005264450.3:c.3324C>T	XP_005264507.2:p.Phe1108=
XM_005264450.4:c.3324C>T	XP_005264507.2:p.Phe1108=
XM_005264451.3:c.3324C>T	XP_005264508.2:p.Phe1108=
XM_005264451.4:c.3324C>T	XP_005264508.2:p.Phe1108=
XM_005264452.3:c.3324C>T	XP_005264509.2:p.Phe1108=
XM_005264452.4:c.3324C>T	XP_005264509.2:p.Phe1108=
XM_005264453.3:c.3324C>T	XP_005264510.2:p.Phe1108=
XM_005264453.4:c.3324C>T	XP_005264510.2:p.Phe1108=
XM_005264454.3:c.3324C>T	XP_005264511.2:p.Phe1108=
XM_005264454.5:c.3324C>T	XP_005264511.2:p.Phe1108=
XM_005264455.3:c.3324C>T	XP_005264512.2:p.Phe1108=
XM_005264455.4:c.3324C>T	XP_005264512.2:p.Phe1108=
XM_006712054.2:c.3324C>T	XP_006712117.1:p.Phe1108=
XM_006712054.3:c.3324C>T	XP_006712117.1:p.Phe1108=
XM_006712055.2:c.3324C>T	XP_006712118.1:p.Phe1108=
XM_006712055.3:c.3324C>T	XP_006712118.1:p.Phe1108=
XM_006712056.2:c.3324C>T	XP_006712119.1:p.Phe1108=
XM_006712056.3:c.3324C>T	XP_006712119.1:p.Phe1108=
XM_006712057.2:c.3324C>T	XP_006712120.1:p.Phe1108=
XM_011533003.1:c.3009C>T	XP_011531305.1:p.Phe1003=
XM_011533003.2:c.3009C>T	XP_011531305.1:p.Phe1003=
XM_011533004.1:c.3324C>T	XP_011531306.1:p.Phe1108=
XM_011533005.1:c.3324C>T	XP_011531307.1:p.Phe1108=
XM_011533005.2:c.3324C>T	XP_011531307.1:p.Phe1108=
XM_017004556.1:c.3324C>T	XP_016860045.1:p.Phe1108=
XM_017004557.1:c.3324C>T	XP_016860046.1:p.Phe1108=
XM_017004558.1:c.3324C>T	XP_016860047.1:p.Phe1108=
XM_017004559.1:c.3324C>T	XP_016860048.1:p.Phe1108=
XM_017004560.1:c.3324C>T	XP_016860049.1:p.Phe1108=
XR_001738858.2:n.3579C>T
XR_244950.3:n.3354C>T
XR_244950.4:n.3579C>T