Canonical Allele Identifier: CA2806037426
Gene: ABCC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.16150857_16150858del , CM000678.2:g.16150857_16150858del GRCh38
NC_000016.9:g.16244714_16244715del , CM000678.1:g.16244714_16244715del GRCh37
NC_000016.8:g.16152215_16152216del NCBI36
NG_007558.2:g.77614_77615del
NG_007558.3:g.77760_77761del

Transcript Alleles

HGVS Amino-acid Change
ENST00000622290.5:c.*381-86_*381-85del ENSP00000483331.2:n.*381-86_*381-85del
ENST00000205557.12:c.4209-86_4209-85del MANE Select ENSP00000205557.7:n.4209-86_4209-85del
ENST00000640696.1:c.1023-86_1023-85del ENSP00000492197.1:n.1023-86_1023-85del
ENST00000205557.11:c.4209-86_4209-85del ENSP00000205557.7:n.4209-86_4209-85del
ENST00000456970.6:c.3834-86_3834-85del ENSP00000405002.2:n.3834-86_3834-85del
ENST00000576204.5:n.1072-86_1072-85del
ENST00000622290.4:c.*1418-86_*1418-85del ENSP00000483331.1:n.*1418-86_*1418-85del
NM_001171.5:c.4209-86_4209-85del NP_001162.4:n.4209-86_4209-85del
XM_011522479.1:c.4176-86_4176-85del XP_011520781.1:n.4176-86_4176-85del
XM_011522480.1:c.3867-86_3867-85del XP_011520782.1:n.3867-86_3867-85del
XM_011522481.1:c.3867-86_3867-85del XP_011520783.1:n.3867-86_3867-85del
XR_933134.1:n.538+6567_538+6568del
NM_001351800.1:c.3867-86_3867-85del NP_001338729.1:n.3867-86_3867-85del
NR_147784.1:n.3871-86_3871-85del
XM_011522479.2:c.4176-86_4176-85del XP_011520781.1:n.4176-86_4176-85del
XM_011522481.3:c.3867-86_3867-85del XP_011520783.1:n.3867-86_3867-85del
XM_017023212.1:c.4041-86_4041-85del XP_016878701.1:n.4041-86_4041-85del
XM_024450261.1:c.4245-86_4245-85del XP_024306029.1:n.4245-86_4245-85del
NM_001171.6:c.4209-86_4209-85del MANE Select NP_001162.5:n.4209-86_4209-85del