Canonical Allele Identifier: CA278631775
Gene: ABCC6 HGNC NCBI

Linked Data

dbSNP Id: rs35199745

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.16163252dup , CM000678.2:g.16163252dup GRCh38
NC_000016.9:g.16257109dup , CM000678.1:g.16257109dup GRCh37
NC_000016.8:g.16164610dup NCBI36
NG_007558.2:g.65221dup
NG_007558.3:g.65367dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000622290.5:c.3307-59dup ENSP00000483331.2:n.3307-59dup
ENST00000205557.12:c.3307-59dup MANE Select ENSP00000205557.7:n.3307-59dup
ENST00000640696.1:c.321-1687dup ENSP00000492197.1:n.321-1687dup
ENST00000205557.11:c.3307-59dup ENSP00000205557.7:n.3307-59dup
ENST00000456970.6:c.3132-1687dup ENSP00000405002.2:n.3132-1687dup
ENST00000622290.4:c.*516-59dup ENSP00000483331.1:n.*516-59dup
NM_001171.5:c.3307-59dup NP_001162.4:n.3307-59dup
XM_011522479.1:c.3274-59dup XP_011520781.1:n.3274-59dup
XM_011522480.1:c.2965-59dup XP_011520782.1:n.2965-59dup
XM_011522481.1:c.2965-59dup XP_011520783.1:n.2965-59dup
XR_932836.1:n.3542-59dup
XR_932837.1:n.3543-1687dup
XR_932838.1:n.3543-1687dup
XR_933133.1:n.407+409dup
XR_933134.1:n.754+409dup
NM_001351800.1:c.2965-59dup NP_001338729.1:n.2965-59dup
NR_147784.1:n.3169-1687dup
XM_011522479.2:c.3274-59dup XP_011520781.1:n.3274-59dup
XM_011522481.3:c.2965-59dup XP_011520783.1:n.2965-59dup
XM_017023212.1:c.3139-59dup XP_016878701.1:n.3139-59dup
XM_017023214.1:c.3307-1687dup XP_016878703.1:n.3307-1687dup
XM_024450261.1:c.3343-59dup XP_024306029.1:n.3343-59dup
XR_932836.2:n.3488-59dup
XR_932837.3:n.3488-1687dup
XR_932838.3:n.3488-1687dup
NM_001171.6:c.3307-59dup MANE Select NP_001162.5:n.3307-59dup