Canonical Allele Identifier: CA2631963599
Gene: ABCC6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.16150785_16150793del , CM000678.2:g.16150785_16150793del GRCh38
NC_000016.9:g.16244642_16244650del , CM000678.1:g.16244642_16244650del GRCh37
NC_000016.8:g.16152143_16152151del NCBI36
NG_007558.2:g.77682_77690del
NG_007558.3:g.77828_77836del

Transcript Alleles

HGVS Amino-acid Change
ENST00000622290.5:c.*381-18_*381-10del ENSP00000483331.2:n.*381-18_*381-10del
ENST00000205557.12:c.4209-18_4209-10del MANE Select ENSP00000205557.7:n.4209-18_4209-10del
ENST00000640696.1:c.1023-18_1023-10del ENSP00000492197.1:n.1023-18_1023-10del
ENST00000205557.11:c.4209-18_4209-10del ENSP00000205557.7:n.4209-18_4209-10del
ENST00000456970.6:c.3834-18_3834-10del ENSP00000405002.2:n.3834-18_3834-10del
ENST00000576204.5:n.1072-18_1072-10del
ENST00000622290.4:c.*1418-18_*1418-10del ENSP00000483331.1:n.*1418-18_*1418-10del
NM_001171.5:c.4209-18_4209-10del NP_001162.4:n.4209-18_4209-10del
XM_011522479.1:c.4176-18_4176-10del XP_011520781.1:n.4176-18_4176-10del
XM_011522480.1:c.3867-18_3867-10del XP_011520782.1:n.3867-18_3867-10del
XM_011522481.1:c.3867-18_3867-10del XP_011520783.1:n.3867-18_3867-10del
XR_933134.1:n.538+6495_538+6503del
NM_001351800.1:c.3867-18_3867-10del NP_001338729.1:n.3867-18_3867-10del
NR_147784.1:n.3871-18_3871-10del
XM_011522479.2:c.4176-18_4176-10del XP_011520781.1:n.4176-18_4176-10del
XM_011522481.3:c.3867-18_3867-10del XP_011520783.1:n.3867-18_3867-10del
XM_017023212.1:c.4041-18_4041-10del XP_016878701.1:n.4041-18_4041-10del
XM_024450261.1:c.4245-18_4245-10del XP_024306029.1:n.4245-18_4245-10del
NM_001171.6:c.4209-18_4209-10del MANE Select NP_001162.5:n.4209-18_4209-10del