Canonical Allele Identifier: CA1605623

Gene: BIRC6

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32597959T>C , CM000664.2:g.32597959T>C	GRCh38
NC_000002.11:g.32823026T>C , CM000664.1:g.32823026T>C	GRCh37
NC_000002.10:g.32676530T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700518.1:c.13770T>C	ENSP00000515025.1:p.Asp4590=
ENST00000700519.1:c.13761T>C	ENSP00000515026.1:p.Asp4587=
ENST00000421745.7:c.13821T>C MANE Select	ENSP00000393596.2:p.Asp4607=
ENST00000421745.6:c.13821T>C	ENSP00000393596.2:p.Asp4607=
ENST00000471232.5:n.2501T>C
NM_016252.3:c.13821T>C	NP_057336.3:p.Asp4607=
XM_005264449.3:c.13902T>C	XP_005264506.2:p.Asp4634=
XM_005264450.3:c.13890T>C	XP_005264507.2:p.Asp4630=
XM_005264451.3:c.13875T>C	XP_005264508.2:p.Asp4625=
XM_005264452.3:c.13860T>C	XP_005264509.2:p.Asp4620=
XM_005264453.3:c.13833T>C	XP_005264510.2:p.Asp4611=
XM_005264454.3:c.13791T>C	XP_005264511.2:p.Asp4597=
XM_005264455.3:c.13770T>C	XP_005264512.2:p.Asp4590=
XM_006712054.2:c.13884T>C	XP_006712117.1:p.Asp4628=
XM_006712055.2:c.13842T>C	XP_006712118.1:p.Asp4614=
XM_006712056.2:c.13803T>C	XP_006712119.1:p.Asp4601=
XM_006712057.2:c.13686T>C	XP_006712120.1:p.Asp4562=
XM_011533003.1:c.13587T>C	XP_011531305.1:p.Asp4529=
XM_011533004.1:c.13902T>C	XP_011531306.1:p.Asp4634=
XR_244950.3:n.14105T>C
XM_005264449.4:c.13902T>C	XP_005264506.2:p.Asp4634=
XM_005264450.4:c.13890T>C	XP_005264507.2:p.Asp4630=
XM_005264451.4:c.13875T>C	XP_005264508.2:p.Asp4625=
XM_005264452.4:c.13860T>C	XP_005264509.2:p.Asp4620=
XM_005264453.4:c.13833T>C	XP_005264510.2:p.Asp4611=
XM_005264454.5:c.13791T>C	XP_005264511.2:p.Asp4597=
XM_005264455.4:c.13770T>C	XP_005264512.2:p.Asp4590=
XM_006712054.3:c.13884T>C	XP_006712117.1:p.Asp4628=
XM_006712055.3:c.13842T>C	XP_006712118.1:p.Asp4614=
XM_006712056.3:c.13803T>C	XP_006712119.1:p.Asp4601=
XM_011533003.2:c.13587T>C	XP_011531305.1:p.Asp4529=
XM_017004556.1:c.13824T>C	XP_016860045.1:p.Asp4608=
XM_017004557.1:c.13791T>C	XP_016860046.1:p.Asp4597=
XM_017004558.1:c.13761T>C	XP_016860047.1:p.Asp4587=
XM_017004559.1:c.13902T>C	XP_016860048.1:p.Asp4634=
XR_001738858.2:n.14219T>C
XR_244950.4:n.14330T>C
NM_001378125.1:c.13818T>C	NP_001365054.1:p.Asp4606=
NM_016252.4:c.13821T>C MANE Select	NP_057336.3:p.Asp4607=