Canonical Allele Identifier: CA2210140951
Gene: ABCC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.16154938C= , CM000678.2:g.16154938C= GRCh38
NC_000016.9:g.16248795C= , CM000678.1:g.16248795C= GRCh37
NC_000016.8:g.16156296C= NCBI36
NG_007558.2:g.73534G=
NG_007558.3:g.73680G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000576204.6:n.839G=
ENST00000622290.5:c.*148G= ENSP00000483331.2:n.*148G=
ENST00000205557.12:c.3976G= MANE Select ENSP00000205557.7:p.Asp1326=
ENST00000640696.1:c.790G= ENSP00000492197.1:p.Asp264=
ENST00000205557.11:c.3976G= ENSP00000205557.7:p.Asp1326=
ENST00000456970.6:c.3601G= ENSP00000405002.2:n.3601G=
ENST00000576204.5:n.839G=
ENST00000622290.4:c.*1185G= ENSP00000483331.1:n.*1185G=
NM_001171.5:c.3976G= NP_001162.4:p.Asp1326=
XM_011522479.1:c.3943G= XP_011520781.1:p.Asp1315=
XM_011522480.1:c.3634G= XP_011520782.1:p.Asp1212=
XM_011522481.1:c.3634G= XP_011520783.1:p.Asp1212=
XR_933134.1:n.539-4843C=
NM_001351800.1:c.3634G= NP_001338729.1:p.Asp1212=
NR_147784.1:n.3638G=
XM_011522479.2:c.3943G= XP_011520781.1:p.Asp1315=
XM_011522481.3:c.3634G= XP_011520783.1:p.Asp1212=
XM_017023212.1:c.3808G= XP_016878701.1:p.Asp1270=
XM_024450261.1:c.4012G= XP_024306029.1:p.Asp1338=
NM_001171.6:c.3976G= MANE Select NP_001162.5:p.Asp1326=