Canonical Allele Identifier: CA2210140967
Gene: ABCC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.16154958G= , CM000678.2:g.16154958G= GRCh38
NC_000016.9:g.16248815G= , CM000678.1:g.16248815G= GRCh37
NC_000016.8:g.16156316G= NCBI36
NG_007558.2:g.73514C=
NG_007558.3:g.73660C=

Transcript Alleles

HGVS Amino-acid change
ENST00000576204.6:n.819C=
ENST00000622290.5:c.*128C= ENSP00000483331.2:n.*128C=
ENST00000205557.12:c.3956C= MANE Select ENSP00000205557.7:p.Ala1319=
ENST00000640696.1:c.770C= ENSP00000492197.1:p.Ala257=
ENST00000205557.11:c.3956C= ENSP00000205557.7:p.Ala1319=
ENST00000456970.6:c.3581C= ENSP00000405002.2:n.3581C=
ENST00000576204.5:n.819C=
ENST00000622290.4:c.*1165C= ENSP00000483331.1:n.*1165C=
NM_001171.5:c.3956C= NP_001162.4:p.Ala1319=
XM_011522479.1:c.3923C= XP_011520781.1:p.Ala1308=
XM_011522480.1:c.3614C= XP_011520782.1:p.Ala1205=
XM_011522481.1:c.3614C= XP_011520783.1:p.Ala1205=
XR_932836.1:n.4254C=
XR_932837.1:n.3992C=
XR_932838.1:n.4055C=
XR_933134.1:n.539-4823G=
NM_001351800.1:c.3614C= NP_001338729.1:p.Ala1205=
NR_147784.1:n.3618C=
XM_011522479.2:c.3923C= XP_011520781.1:p.Ala1308=
XM_011522481.3:c.3614C= XP_011520783.1:p.Ala1205=
XM_017023212.1:c.3788C= XP_016878701.1:p.Ala1263=
XM_024450261.1:c.3992C= XP_024306029.1:p.Ala1331=
XR_932837.3:n.3937C=
NM_001171.6:c.3956C= MANE Select NP_001162.5:p.Ala1319=