Canonical Allele Identifier: CA2631963638
Gene: ABCC6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.16150804_16150806dup , CM000678.2:g.16150804_16150806dup GRCh38
NC_000016.9:g.16244661_16244663dup , CM000678.1:g.16244661_16244663dup GRCh37
NC_000016.8:g.16152162_16152164dup NCBI36
NG_007558.2:g.77666_77668dup
NG_007558.3:g.77812_77814dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000622290.5:c.*381-34_*381-32dup ENSP00000483331.2:n.*381-34_*381-32dup
ENST00000205557.12:c.4209-34_4209-32dup MANE Select ENSP00000205557.7:n.4209-34_4209-32dup
ENST00000640696.1:c.1023-34_1023-32dup ENSP00000492197.1:n.1023-34_1023-32dup
ENST00000205557.11:c.4209-34_4209-32dup ENSP00000205557.7:n.4209-34_4209-32dup
ENST00000456970.6:c.3834-34_3834-32dup ENSP00000405002.2:n.3834-34_3834-32dup
ENST00000576204.5:n.1072-34_1072-32dup
ENST00000622290.4:c.*1418-34_*1418-32dup ENSP00000483331.1:n.*1418-34_*1418-32dup
NM_001171.5:c.4209-34_4209-32dup NP_001162.4:n.4209-34_4209-32dup
XM_011522479.1:c.4176-34_4176-32dup XP_011520781.1:n.4176-34_4176-32dup
XM_011522480.1:c.3867-34_3867-32dup XP_011520782.1:n.3867-34_3867-32dup
XM_011522481.1:c.3867-34_3867-32dup XP_011520783.1:n.3867-34_3867-32dup
XR_933134.1:n.538+6514_538+6516dup
NM_001351800.1:c.3867-34_3867-32dup NP_001338729.1:n.3867-34_3867-32dup
NR_147784.1:n.3871-34_3871-32dup
XM_011522479.2:c.4176-34_4176-32dup XP_011520781.1:n.4176-34_4176-32dup
XM_011522481.3:c.3867-34_3867-32dup XP_011520783.1:n.3867-34_3867-32dup
XM_017023212.1:c.4041-34_4041-32dup XP_016878701.1:n.4041-34_4041-32dup
XM_024450261.1:c.4245-34_4245-32dup XP_024306029.1:n.4245-34_4245-32dup
NM_001171.6:c.4209-34_4209-32dup MANE Select NP_001162.5:n.4209-34_4209-32dup