Canonical Allele Identifier: CA2806038042
Gene: ABCC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.16155172_16155173insAGT , CM000678.2:g.16155172_16155173insAGT GRCh38
NC_000016.9:g.16249029_16249030insAGT , CM000678.1:g.16249029_16249030insAGT GRCh37
NC_000016.8:g.16156530_16156531insAGT NCBI36
NG_007558.2:g.73299_73300insACT
NG_007558.3:g.73445_73446insACT

Transcript Alleles

HGVS Amino-acid Change
ENST00000576204.6:n.604_605insACT
ENST00000622290.5:c.*55-142_*55-141insACT ENSP00000483331.2:n.*55-142_*55-141insACT
ENST00000205557.12:c.3883-142_3883-141insACT MANE Select ENSP00000205557.7:n.3883-142_3883-141insACT
ENST00000640696.1:c.697-142_697-141insACT ENSP00000492197.1:n.697-142_697-141insACT
ENST00000205557.11:c.3883-142_3883-141insACT ENSP00000205557.7:n.3883-142_3883-141insACT
ENST00000456970.6:c.3508-142_3508-141insACT ENSP00000405002.2:n.3508-142_3508-141insACT
ENST00000576204.5:n.604_605insACT
ENST00000622290.4:c.*1092-142_*1092-141insACT ENSP00000483331.1:n.*1092-142_*1092-141insACT
NM_001171.5:c.3883-142_3883-141insACT NP_001162.4:n.3883-142_3883-141insACT
XM_011522479.1:c.3850-142_3850-141insACT XP_011520781.1:n.3850-142_3850-141insACT
XM_011522480.1:c.3541-142_3541-141insACT XP_011520782.1:n.3541-142_3541-141insACT
XM_011522481.1:c.3541-142_3541-141insACT XP_011520783.1:n.3541-142_3541-141insACT
XR_932836.1:n.4181-142_4181-141insACT
XR_932837.1:n.3919-142_3919-141insACT
XR_932838.1:n.3982-142_3982-141insACT
XR_933134.1:n.539-4609_539-4608insAGT
NM_001351800.1:c.3541-142_3541-141insACT NP_001338729.1:n.3541-142_3541-141insACT
NR_147784.1:n.3545-142_3545-141insACT
XM_011522479.2:c.3850-142_3850-141insACT XP_011520781.1:n.3850-142_3850-141insACT
XM_011522481.3:c.3541-142_3541-141insACT XP_011520783.1:n.3541-142_3541-141insACT
XM_017023212.1:c.3715-142_3715-141insACT XP_016878701.1:n.3715-142_3715-141insACT
XM_024450261.1:c.3919-142_3919-141insACT XP_024306029.1:n.3919-142_3919-141insACT
XR_932836.2:n.4127-142_4127-141insACT
XR_932837.3:n.3864-142_3864-141insACT
XR_932838.3:n.3927-142_3927-141insACT
NM_001171.6:c.3883-142_3883-141insACT MANE Select NP_001162.5:n.3883-142_3883-141insACT