Canonical Allele Identifier: CA346531064
Gene: BIRC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.32508117C>T , CM000664.2:g.32508117C>T GRCh38
NC_000002.11:g.32733184C>T , CM000664.1:g.32733184C>T GRCh37
NC_000002.10:g.32586688C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000700518.1:c.9787C>T ENSP00000515025.1:p.Leu3263Phe
ENST00000700519.1:c.9778C>T ENSP00000515026.1:p.Leu3260Phe
ENST00000421745.7:c.9838C>T MANE Select ENSP00000393596.2:p.Leu3280Phe
ENST00000648282.1:c.9624C>T
ENST00000421745.6:c.9838C>T ENSP00000393596.2:p.Leu3280Phe
NM_016252.3:c.9838C>T NP_057336.3:p.Leu3280Phe
XM_005264449.3:c.9919C>T XP_005264506.2:p.Leu3307Phe
XM_005264450.3:c.9907C>T XP_005264507.2:p.Leu3303Phe
XM_005264451.3:c.9892C>T XP_005264508.2:p.Leu3298Phe
XM_005264452.3:c.9877C>T XP_005264509.2:p.Leu3293Phe
XM_005264453.3:c.9850C>T XP_005264510.2:p.Leu3284Phe
XM_005264454.3:c.9919C>T XP_005264511.2:p.Leu3307Phe
XM_005264455.3:c.9787C>T XP_005264512.2:p.Leu3263Phe
XM_006712054.2:c.9901C>T XP_006712117.1:p.Leu3301Phe
XM_006712055.2:c.9919C>T XP_006712118.1:p.Leu3307Phe
XM_006712056.2:c.9820C>T XP_006712119.1:p.Leu3274Phe
XM_006712057.2:c.9703C>T XP_006712120.1:p.Leu3235Phe
XM_011533003.1:c.9604C>T XP_011531305.1:p.Leu3202Phe
XM_011533004.1:c.9919C>T XP_011531306.1:p.Leu3307Phe
XM_011533005.1:c.9919C>T XP_011531307.1:p.Leu3307Phe
XR_244950.3:n.9949C>T
XM_005264449.4:c.9919C>T XP_005264506.2:p.Leu3307Phe
XM_005264450.4:c.9907C>T XP_005264507.2:p.Leu3303Phe
XM_005264451.4:c.9892C>T XP_005264508.2:p.Leu3298Phe
XM_005264452.4:c.9877C>T XP_005264509.2:p.Leu3293Phe
XM_005264453.4:c.9850C>T XP_005264510.2:p.Leu3284Phe
XM_005264454.5:c.9919C>T XP_005264511.2:p.Leu3307Phe
XM_005264455.4:c.9787C>T XP_005264512.2:p.Leu3263Phe
XM_006712054.3:c.9901C>T XP_006712117.1:p.Leu3301Phe
XM_006712055.3:c.9919C>T XP_006712118.1:p.Leu3307Phe
XM_006712056.3:c.9820C>T XP_006712119.1:p.Leu3274Phe
XM_011533003.2:c.9604C>T XP_011531305.1:p.Leu3202Phe
XM_011533005.2:c.9919C>T XP_011531307.1:p.Leu3307Phe
XM_017004556.1:c.9901C>T XP_016860045.1:p.Leu3301Phe
XM_017004557.1:c.9808C>T XP_016860046.1:p.Leu3270Phe
XM_017004558.1:c.9778C>T XP_016860047.1:p.Leu3260Phe
XM_017004559.1:c.9919C>T XP_016860048.1:p.Leu3307Phe
XM_017004560.1:c.9901C>T XP_016860049.1:p.Leu3301Phe
XR_001738858.2:n.10174C>T
XR_244950.4:n.10174C>T
NM_001378125.1:c.9835C>T NP_001365054.1:p.Leu3279Phe
NM_016252.4:c.9838C>T MANE Select NP_057336.3:p.Leu3280Phe