Canonical Allele Identifier: CA281575
Gene: ABCC6 HGNC NCBI

Linked Data

ClinVar Variation Id: 6572
dbSNP Id: rs72653744
COSMIC: COSM471371

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.16163009G>A , CM000678.2:g.16163009G>A GRCh38
NC_000016.9:g.16256866G>A , CM000678.1:g.16256866G>A GRCh37
NC_000016.8:g.16164367G>A NCBI36
NG_007558.2:g.65463C>T
NG_007558.3:g.65609C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000622290.5:c.3490C>T ENSP00000483331.2:p.Arg1164Ter
ENST00000205557.12:c.3490C>T MANE Select ENSP00000205557.7:p.Arg1164Ter
ENST00000640696.1:c.321-1445C>T ENSP00000492197.1:n.321-1445C>T
ENST00000205557.11:c.3490C>T ENSP00000205557.7:p.Arg1164Ter
ENST00000456970.6:c.3132-1445C>T ENSP00000405002.2:n.3132-1445C>T
ENST00000622290.4:c.*699C>T ENSP00000483331.1:n.*699C>T
NM_001171.5:c.3490C>T NP_001162.4:p.Arg1164Ter
XM_011522479.1:c.3457C>T XP_011520781.1:p.Arg1153Ter
XM_011522480.1:c.3148C>T XP_011520782.1:p.Arg1050Ter
XM_011522481.1:c.3148C>T XP_011520783.1:p.Arg1050Ter
XR_932836.1:n.3725C>T
XR_932837.1:n.3543-1445C>T
XR_932838.1:n.3543-1445C>T
XR_933133.1:n.407+166G>A
XR_933134.1:n.754+166G>A
NM_001351800.1:c.3148C>T NP_001338729.1:p.Arg1050Ter
NR_147784.1:n.3169-1445C>T
XM_011522479.2:c.3457C>T XP_011520781.1:p.Arg1153Ter
XM_011522481.3:c.3148C>T XP_011520783.1:p.Arg1050Ter
XM_017023212.1:c.3322C>T XP_016878701.1:p.Arg1108Ter
XM_017023214.1:c.3307-1445C>T XP_016878703.1:n.3307-1445C>T
XM_024450261.1:c.3526C>T XP_024306029.1:p.Arg1176Ter
XR_932836.2:n.3671C>T
XR_932837.3:n.3488-1445C>T
XR_932838.3:n.3488-1445C>T
NM_001171.6:c.3490C>T MANE Select NP_001162.5:p.Arg1164Ter