Canonical Allele Identifier: CA281573
Gene: ABCC6 HGNC NCBI

Linked Data

ClinVar Variation Id: 6571
dbSNP Id: rs28939701

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.16163087G>A , CM000678.2:g.16163087G>A GRCh38
NC_000016.9:g.16256944G>A , CM000678.1:g.16256944G>A GRCh37
NC_000016.8:g.16164445G>A NCBI36
NG_007558.2:g.65385C>T
NG_007558.3:g.65531C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000622290.5:c.3412C>T ENSP00000483331.2:p.Arg1138Trp
ENST00000205557.12:c.3412C>T MANE Select ENSP00000205557.7:p.Arg1138Trp
ENST00000640696.1:c.321-1523C>T ENSP00000492197.1:n.321-1523C>T
ENST00000205557.11:c.3412C>T ENSP00000205557.7:p.Arg1138Trp
ENST00000456970.6:c.3132-1523C>T ENSP00000405002.2:n.3132-1523C>T
ENST00000622290.4:c.*621C>T ENSP00000483331.1:n.*621C>T
NM_001171.5:c.3412C>T NP_001162.4:p.Arg1138Trp
XM_011522479.1:c.3379C>T XP_011520781.1:p.Arg1127Trp
XM_011522480.1:c.3070C>T XP_011520782.1:p.Arg1024Trp
XM_011522481.1:c.3070C>T XP_011520783.1:p.Arg1024Trp
XR_932836.1:n.3647C>T
XR_932837.1:n.3543-1523C>T
XR_932838.1:n.3543-1523C>T
XR_933133.1:n.407+244G>A
XR_933134.1:n.754+244G>A
NM_001351800.1:c.3070C>T NP_001338729.1:p.Arg1024Trp
NR_147784.1:n.3169-1523C>T
XM_011522479.2:c.3379C>T XP_011520781.1:p.Arg1127Trp
XM_011522481.3:c.3070C>T XP_011520783.1:p.Arg1024Trp
XM_017023212.1:c.3244C>T XP_016878701.1:p.Arg1082Trp
XM_017023214.1:c.3307-1523C>T XP_016878703.1:n.3307-1523C>T
XM_024450261.1:c.3448C>T XP_024306029.1:p.Arg1150Trp
XR_932836.2:n.3593C>T
XR_932837.3:n.3488-1523C>T
XR_932838.3:n.3488-1523C>T
NM_001171.6:c.3412C>T MANE Select NP_001162.5:p.Arg1138Trp