Canonical Allele Identifier: CA2631959588
Gene: ABCC6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.16155162_16155163del , CM000678.2:g.16155162_16155163del GRCh38
NC_000016.9:g.16249019_16249020del , CM000678.1:g.16249019_16249020del GRCh37
NC_000016.8:g.16156520_16156521del NCBI36
NG_007558.2:g.73314_73315del
NG_007558.3:g.73460_73461del

Transcript Alleles

HGVS Amino-acid Change
ENST00000576204.6:n.619_620del
ENST00000622290.5:c.*55-127_*55-126del ENSP00000483331.2:n.*55-127_*55-126del
ENST00000205557.12:c.3883-127_3883-126del MANE Select ENSP00000205557.7:n.3883-127_3883-126del
ENST00000640696.1:c.697-127_697-126del ENSP00000492197.1:n.697-127_697-126del
ENST00000205557.11:c.3883-127_3883-126del ENSP00000205557.7:n.3883-127_3883-126del
ENST00000456970.6:c.3508-127_3508-126del ENSP00000405002.2:n.3508-127_3508-126del
ENST00000576204.5:n.619_620del
ENST00000622290.4:c.*1092-127_*1092-126del ENSP00000483331.1:n.*1092-127_*1092-126del
NM_001171.5:c.3883-127_3883-126del NP_001162.4:n.3883-127_3883-126del
XM_011522479.1:c.3850-127_3850-126del XP_011520781.1:n.3850-127_3850-126del
XM_011522480.1:c.3541-127_3541-126del XP_011520782.1:n.3541-127_3541-126del
XM_011522481.1:c.3541-127_3541-126del XP_011520783.1:n.3541-127_3541-126del
XR_932836.1:n.4181-127_4181-126del
XR_932837.1:n.3919-127_3919-126del
XR_932838.1:n.3982-127_3982-126del
XR_933134.1:n.539-4619_539-4618del
NM_001351800.1:c.3541-127_3541-126del NP_001338729.1:n.3541-127_3541-126del
NR_147784.1:n.3545-127_3545-126del
XM_011522479.2:c.3850-127_3850-126del XP_011520781.1:n.3850-127_3850-126del
XM_011522481.3:c.3541-127_3541-126del XP_011520783.1:n.3541-127_3541-126del
XM_017023212.1:c.3715-127_3715-126del XP_016878701.1:n.3715-127_3715-126del
XM_024450261.1:c.3919-127_3919-126del XP_024306029.1:n.3919-127_3919-126del
XR_932836.2:n.4127-127_4127-126del
XR_932837.3:n.3864-127_3864-126del
XR_932838.3:n.3927-127_3927-126del
NM_001171.6:c.3883-127_3883-126del MANE Select NP_001162.5:n.3883-127_3883-126del