Canonical Allele Identifier: CA2210140975
Gene: ABCC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.16154962C= , CM000678.2:g.16154962C= GRCh38
NC_000016.9:g.16248819C= , CM000678.1:g.16248819C= GRCh37
NC_000016.8:g.16156320C= NCBI36
NG_007558.2:g.73510G=
NG_007558.3:g.73656G=

Transcript Alleles

HGVS Amino-acid change
ENST00000576204.6:n.815G=
ENST00000622290.5:c.*124G= ENSP00000483331.2:n.*124G=
ENST00000205557.12:c.3952G= MANE Select ENSP00000205557.7:p.Ala1318=
ENST00000640696.1:c.766G= ENSP00000492197.1:p.Ala256=
ENST00000205557.11:c.3952G= ENSP00000205557.7:p.Ala1318=
ENST00000456970.6:c.3577G= ENSP00000405002.2:n.3577G=
ENST00000576204.5:n.815G=
ENST00000622290.4:c.*1161G= ENSP00000483331.1:n.*1161G=
NM_001171.5:c.3952G= NP_001162.4:p.Ala1318=
XM_011522479.1:c.3919G= XP_011520781.1:p.Ala1307=
XM_011522480.1:c.3610G= XP_011520782.1:p.Ala1204=
XM_011522481.1:c.3610G= XP_011520783.1:p.Ala1204=
XR_932836.1:n.4250G=
XR_932837.1:n.3988G=
XR_932838.1:n.4051G=
XR_933134.1:n.539-4819C=
NM_001351800.1:c.3610G= NP_001338729.1:p.Ala1204=
NR_147784.1:n.3614G=
XM_011522479.2:c.3919G= XP_011520781.1:p.Ala1307=
XM_011522481.3:c.3610G= XP_011520783.1:p.Ala1204=
XM_017023212.1:c.3784G= XP_016878701.1:p.Ala1262=
XM_024450261.1:c.3988G= XP_024306029.1:p.Ala1330=
XR_932837.3:n.3933G=
NM_001171.6:c.3952G= MANE Select NP_001162.5:p.Ala1318=