Canonical Allele Identifier: CA2806038063
Gene: ABCC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.16155182_16155185del , CM000678.2:g.16155182_16155185del GRCh38
NC_000016.9:g.16249039_16249042del , CM000678.1:g.16249039_16249042del GRCh37
NC_000016.8:g.16156540_16156543del NCBI36
NG_007558.2:g.73288_73291del
NG_007558.3:g.73434_73437del

Transcript Alleles

HGVS Amino-acid Change
ENST00000576204.6:n.593_596del
ENST00000622290.5:c.*55-153_*55-150del ENSP00000483331.2:n.*55-153_*55-150del
ENST00000205557.12:c.3883-153_3883-150del MANE Select ENSP00000205557.7:n.3883-153_3883-150del
ENST00000640696.1:c.697-153_697-150del ENSP00000492197.1:n.697-153_697-150del
ENST00000205557.11:c.3883-153_3883-150del ENSP00000205557.7:n.3883-153_3883-150del
ENST00000456970.6:c.3508-153_3508-150del ENSP00000405002.2:n.3508-153_3508-150del
ENST00000576204.5:n.593_596del
ENST00000622290.4:c.*1092-153_*1092-150del ENSP00000483331.1:n.*1092-153_*1092-150del
NM_001171.5:c.3883-153_3883-150del NP_001162.4:n.3883-153_3883-150del
XM_011522479.1:c.3850-153_3850-150del XP_011520781.1:n.3850-153_3850-150del
XM_011522480.1:c.3541-153_3541-150del XP_011520782.1:n.3541-153_3541-150del
XM_011522481.1:c.3541-153_3541-150del XP_011520783.1:n.3541-153_3541-150del
XR_932836.1:n.4181-153_4181-150del
XR_932837.1:n.3919-153_3919-150del
XR_932838.1:n.3982-153_3982-150del
XR_933134.1:n.539-4599_539-4596del
NM_001351800.1:c.3541-153_3541-150del NP_001338729.1:n.3541-153_3541-150del
NR_147784.1:n.3545-153_3545-150del
XM_011522479.2:c.3850-153_3850-150del XP_011520781.1:n.3850-153_3850-150del
XM_011522481.3:c.3541-153_3541-150del XP_011520783.1:n.3541-153_3541-150del
XM_017023212.1:c.3715-153_3715-150del XP_016878701.1:n.3715-153_3715-150del
XM_024450261.1:c.3919-153_3919-150del XP_024306029.1:n.3919-153_3919-150del
XR_932836.2:n.4127-153_4127-150del
XR_932837.3:n.3864-153_3864-150del
XR_932838.3:n.3927-153_3927-150del
NM_001171.6:c.3883-153_3883-150del MANE Select NP_001162.5:n.3883-153_3883-150del