Canonical Allele Identifier: CA2631959410
Gene: ABCC6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.16155053_16155058del , CM000678.2:g.16155053_16155058del GRCh38
NC_000016.9:g.16248910_16248915del , CM000678.1:g.16248910_16248915del GRCh37
NC_000016.8:g.16156411_16156416del NCBI36
NG_007558.2:g.73414_73419del
NG_007558.3:g.73560_73565del

Transcript Alleles

HGVS Amino-acid change
ENST00000576204.6:n.719_724del
ENST00000622290.5:c.*55-27_*55-22del ENSP00000483331.2:n.*55-27_*55-22del
ENST00000205557.12:c.3883-27_3883-22del MANE Select ENSP00000205557.7:n.3883-27_3883-22del
ENST00000640696.1:c.697-27_697-22del ENSP00000492197.1:n.697-27_697-22del
ENST00000205557.11:c.3883-27_3883-22del ENSP00000205557.7:n.3883-27_3883-22del
ENST00000456970.6:c.3508-27_3508-22del ENSP00000405002.2:n.3508-27_3508-22del
ENST00000576204.5:n.719_724del
ENST00000622290.4:c.*1092-27_*1092-22del ENSP00000483331.1:n.*1092-27_*1092-22del
NM_001171.5:c.3883-27_3883-22del NP_001162.4:n.3883-27_3883-22del
XM_011522479.1:c.3850-27_3850-22del XP_011520781.1:n.3850-27_3850-22del
XM_011522480.1:c.3541-27_3541-22del XP_011520782.1:n.3541-27_3541-22del
XM_011522481.1:c.3541-27_3541-22del XP_011520783.1:n.3541-27_3541-22del
XR_932836.1:n.4181-27_4181-22del
XR_932837.1:n.3919-27_3919-22del
XR_932838.1:n.3982-27_3982-22del
XR_933134.1:n.539-4728_539-4723del
NM_001351800.1:c.3541-27_3541-22del NP_001338729.1:n.3541-27_3541-22del
NR_147784.1:n.3545-27_3545-22del
XM_011522479.2:c.3850-27_3850-22del XP_011520781.1:n.3850-27_3850-22del
XM_011522481.3:c.3541-27_3541-22del XP_011520783.1:n.3541-27_3541-22del
XM_017023212.1:c.3715-27_3715-22del XP_016878701.1:n.3715-27_3715-22del
XM_024450261.1:c.3919-27_3919-22del XP_024306029.1:n.3919-27_3919-22del
XR_932836.2:n.4127-27_4127-22del
XR_932837.3:n.3864-27_3864-22del
XR_932838.3:n.3927-27_3927-22del
NM_001171.6:c.3883-27_3883-22del MANE Select NP_001162.5:n.3883-27_3883-22del