Canonical Allele Identifier: CA975113349
Gene: ABCC6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.16197974_16197978dup , CM000678.2:g.16197974_16197978dup GRCh38
NC_000016.9:g.16291831_16291835dup , CM000678.1:g.16291831_16291835dup GRCh37
NC_000016.8:g.16199332_16199336dup NCBI36
NG_007558.2:g.30494_30498dup
NG_007558.3:g.30640_30644dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000574094.6:c.1338+43_1338+47dup ENSP00000507301.1:n.1338+43_1338+47dup
ENST00000622290.5:c.1338+43_1338+47dup ENSP00000483331.2:n.1338+43_1338+47dup
ENST00000205557.12:c.1338+43_1338+47dup MANE Select ENSP00000205557.7:n.1338+43_1338+47dup
ENST00000205557.11:c.1338+43_1338+47dup ENSP00000205557.7:n.1338+43_1338+47dup
ENST00000456970.6:c.1338+43_1338+47dup ENSP00000405002.2:n.1338+43_1338+47dup
ENST00000574094.5:n.1434+43_1434+47dup
ENST00000622290.4:c.1338+43_1338+47dup ENSP00000483331.1:n.1338+43_1338+47dup
NM_001171.5:c.1338+43_1338+47dup NP_001162.4:n.1338+43_1338+47dup
XM_011522479.1:c.1338+43_1338+47dup XP_011520781.1:n.1338+43_1338+47dup
XM_011522480.1:c.996+43_996+47dup XP_011520782.1:n.996+43_996+47dup
XM_011522481.1:c.996+43_996+47dup XP_011520783.1:n.996+43_996+47dup
XM_011522482.1:c.1338+43_1338+47dup XP_011520784.1:n.1338+43_1338+47dup
XR_932836.1:n.1573+43_1573+47dup
XR_932837.1:n.1574+43_1574+47dup
XR_932838.1:n.1574+43_1574+47dup
NM_001351800.1:c.996+43_996+47dup NP_001338729.1:n.996+43_996+47dup
NR_147784.1:n.1375+43_1375+47dup
XM_011522479.2:c.1338+43_1338+47dup XP_011520781.1:n.1338+43_1338+47dup
XM_011522481.3:c.996+43_996+47dup XP_011520783.1:n.996+43_996+47dup
XM_011522482.3:c.1338+43_1338+47dup XP_011520784.1:n.1338+43_1338+47dup
XM_017023212.1:c.1338+43_1338+47dup XP_016878701.1:n.1338+43_1338+47dup
XM_017023214.1:c.1338+43_1338+47dup XP_016878703.1:n.1338+43_1338+47dup
XM_024450261.1:c.1374+43_1374+47dup XP_024306029.1:n.1374+43_1374+47dup
XR_932836.2:n.1519+43_1519+47dup
XR_932837.3:n.1519+43_1519+47dup
XR_932838.3:n.1519+43_1519+47dup
NM_001171.6:c.1338+43_1338+47dup MANE Select NP_001162.5:n.1338+43_1338+47dup