Canonical Allele Identifier: CA278625843
Gene: ABCC6 HGNC NCBI

Linked Data

dbSNP Id: rs113534366

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.16155258_16155259del , CM000678.2:g.16155258_16155259del GRCh38
NC_000016.9:g.16249115_16249116del , CM000678.1:g.16249115_16249116del GRCh37
NC_000016.8:g.16156616_16156617del NCBI36
NG_007558.2:g.73219_73220del
NG_007558.3:g.73365_73366del

Transcript Alleles

HGVS Amino-acid Change
ENST00000576204.6:n.524_525del
ENST00000622290.5:c.*55-222_*55-221del ENSP00000483331.2:n.*55-222_*55-221del
ENST00000205557.12:c.3883-222_3883-221del MANE Select ENSP00000205557.7:n.3883-222_3883-221del
ENST00000640696.1:c.697-222_697-221del ENSP00000492197.1:n.697-222_697-221del
ENST00000205557.11:c.3883-222_3883-221del ENSP00000205557.7:n.3883-222_3883-221del
ENST00000456970.6:c.3508-222_3508-221del ENSP00000405002.2:n.3508-222_3508-221del
ENST00000576204.5:n.524_525del
ENST00000622290.4:c.*1092-222_*1092-221del ENSP00000483331.1:n.*1092-222_*1092-221del
NM_001171.5:c.3883-222_3883-221del NP_001162.4:n.3883-222_3883-221del
XM_011522479.1:c.3850-222_3850-221del XP_011520781.1:n.3850-222_3850-221del
XM_011522480.1:c.3541-222_3541-221del XP_011520782.1:n.3541-222_3541-221del
XM_011522481.1:c.3541-222_3541-221del XP_011520783.1:n.3541-222_3541-221del
XR_932836.1:n.4181-222_4181-221del
XR_932837.1:n.3919-222_3919-221del
XR_932838.1:n.3982-222_3982-221del
XR_933134.1:n.539-4523_539-4522del
NM_001351800.1:c.3541-222_3541-221del NP_001338729.1:n.3541-222_3541-221del
NR_147784.1:n.3545-222_3545-221del
XM_011522479.2:c.3850-222_3850-221del XP_011520781.1:n.3850-222_3850-221del
XM_011522481.3:c.3541-222_3541-221del XP_011520783.1:n.3541-222_3541-221del
XM_017023212.1:c.3715-222_3715-221del XP_016878701.1:n.3715-222_3715-221del
XM_024450261.1:c.3919-222_3919-221del XP_024306029.1:n.3919-222_3919-221del
XR_932836.2:n.4127-222_4127-221del
XR_932837.3:n.3864-222_3864-221del
XR_932838.3:n.3927-222_3927-221del
NM_001171.6:c.3883-222_3883-221del MANE Select NP_001162.5:n.3883-222_3883-221del