Canonical Allele Identifier: CA2631961851
Gene: ABCC6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.16159433_16159435dup , CM000678.2:g.16159433_16159435dup GRCh38
NC_000016.9:g.16253290_16253292dup , CM000678.1:g.16253290_16253292dup GRCh37
NC_000016.8:g.16160791_16160793dup NCBI36
NG_007558.2:g.69043_69045dup
NG_007558.3:g.69189_69191dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000622290.5:c.3735+53_3735+55dup ENSP00000483331.2:n.3735+53_3735+55dup
ENST00000205557.12:c.3735+53_3735+55dup MANE Select ENSP00000205557.7:n.3735+53_3735+55dup
ENST00000640696.1:c.549+53_549+55dup ENSP00000492197.1:n.549+53_549+55dup
ENST00000205557.11:c.3735+53_3735+55dup ENSP00000205557.7:n.3735+53_3735+55dup
ENST00000456970.6:c.3360+53_3360+55dup ENSP00000405002.2:n.3360+53_3360+55dup
ENST00000622290.4:c.*944+53_*944+55dup ENSP00000483331.1:n.*944+53_*944+55dup
NM_001171.5:c.3735+53_3735+55dup NP_001162.4:n.3735+53_3735+55dup
XM_011522479.1:c.3702+53_3702+55dup XP_011520781.1:n.3702+53_3702+55dup
XM_011522480.1:c.3393+53_3393+55dup XP_011520782.1:n.3393+53_3393+55dup
XM_011522481.1:c.3393+53_3393+55dup XP_011520783.1:n.3393+53_3393+55dup
XR_932836.1:n.3970+53_3970+55dup
XR_932837.1:n.3771+53_3771+55dup
XR_932838.1:n.3771+53_3771+55dup
XR_933134.1:n.539-348_539-346dup
NM_001351800.1:c.3393+53_3393+55dup NP_001338729.1:n.3393+53_3393+55dup
NR_147784.1:n.3397+53_3397+55dup
XM_011522479.2:c.3702+53_3702+55dup XP_011520781.1:n.3702+53_3702+55dup
XM_011522481.3:c.3393+53_3393+55dup XP_011520783.1:n.3393+53_3393+55dup
XM_017023212.1:c.3567+53_3567+55dup XP_016878701.1:n.3567+53_3567+55dup
XM_024450261.1:c.3771+53_3771+55dup XP_024306029.1:n.3771+53_3771+55dup
XR_932836.2:n.3916+53_3916+55dup
XR_932837.3:n.3716+53_3716+55dup
XR_932838.3:n.3716+53_3716+55dup
NM_001171.6:c.3735+53_3735+55dup MANE Select NP_001162.5:n.3735+53_3735+55dup