Canonical Allele Identifier: CA394884414
Gene: ABCC6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.16169702T>G , CM000678.2:g.16169702T>G GRCh38
NC_000016.9:g.16263559T>G , CM000678.1:g.16263559T>G GRCh37
NC_000016.8:g.16171060T>G NCBI36
NG_007558.2:g.58770A>C
NG_007558.3:g.58916A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000622290.5:c.2939A>C ENSP00000483331.2:p.Gln980Pro
ENST00000205557.12:c.2939A>C MANE Select ENSP00000205557.7:p.Gln980Pro
ENST00000205557.11:c.2939A>C ENSP00000205557.7:p.Gln980Pro
ENST00000456970.6:c.2764A>C ENSP00000405002.2:n.2764A>C
ENST00000622290.4:c.*148A>C ENSP00000483331.1:n.*148A>C
NM_001171.5:c.2939A>C NP_001162.4:p.Gln980Pro
XM_011522479.1:c.2906A>C XP_011520781.1:p.Gln969Pro
XM_011522480.1:c.2597A>C XP_011520782.1:p.Gln866Pro
XM_011522481.1:c.2597A>C XP_011520783.1:p.Gln866Pro
XR_932836.1:n.3174A>C
XR_932837.1:n.3175A>C
XR_932838.1:n.3175A>C
NM_001351800.1:c.2597A>C NP_001338729.1:p.Gln866Pro
NR_147784.1:n.2801A>C
XM_011522479.2:c.2906A>C XP_011520781.1:p.Gln969Pro
XM_011522481.3:c.2597A>C XP_011520783.1:p.Gln866Pro
XM_017023212.1:c.2771A>C XP_016878701.1:p.Gln924Pro
XM_017023214.1:c.2939A>C XP_016878703.1:p.Gln980Pro
XM_024450261.1:c.2975A>C XP_024306029.1:p.Gln992Pro
XR_932836.2:n.3120A>C
XR_932837.3:n.3120A>C
XR_932838.3:n.3120A>C
NM_001171.6:c.2939A>C MANE Select NP_001162.5:p.Gln980Pro