Canonical Allele Identifier: CA394876073
Gene: ABCC6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.16155001T>G , CM000678.2:g.16155001T>G GRCh38
NC_000016.9:g.16248858T>G , CM000678.1:g.16248858T>G GRCh37
NC_000016.8:g.16156359T>G NCBI36
NG_007558.2:g.73471A>C
NG_007558.3:g.73617A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000576204.6:n.776A>C
ENST00000622290.5:c.*85A>C ENSP00000483331.2:n.*85A>C
ENST00000205557.12:c.3913A>C MANE Select ENSP00000205557.7:p.Lys1305Gln
ENST00000640696.1:c.727A>C ENSP00000492197.1:p.Lys243Gln
ENST00000205557.11:c.3913A>C ENSP00000205557.7:p.Lys1305Gln
ENST00000456970.6:c.3538A>C ENSP00000405002.2:n.3538A>C
ENST00000576204.5:n.776A>C
ENST00000622290.4:c.*1122A>C ENSP00000483331.1:n.*1122A>C
NM_001171.5:c.3913A>C NP_001162.4:p.Lys1305Gln
XM_011522479.1:c.3880A>C XP_011520781.1:p.Lys1294Gln
XM_011522480.1:c.3571A>C XP_011520782.1:p.Lys1191Gln
XM_011522481.1:c.3571A>C XP_011520783.1:p.Lys1191Gln
XR_932836.1:n.4211A>C
XR_932837.1:n.3949A>C
XR_932838.1:n.4012A>C
XR_933134.1:n.539-4780T>G
NM_001351800.1:c.3571A>C NP_001338729.1:p.Lys1191Gln
NR_147784.1:n.3575A>C
XM_011522479.2:c.3880A>C XP_011520781.1:p.Lys1294Gln
XM_011522481.3:c.3571A>C XP_011520783.1:p.Lys1191Gln
XM_017023212.1:c.3745A>C XP_016878701.1:p.Lys1249Gln
XM_024450261.1:c.3949A>C XP_024306029.1:p.Lys1317Gln
XR_932836.2:n.4157A>C
XR_932837.3:n.3894A>C
XR_932838.3:n.3957A>C
NM_001171.6:c.3913A>C MANE Select NP_001162.5:p.Lys1305Gln