Canonical Allele Identifier: CA2806038084
Gene: ABCC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.16155196_16155197insAGT , CM000678.2:g.16155196_16155197insAGT GRCh38
NC_000016.9:g.16249053_16249054insAGT , CM000678.1:g.16249053_16249054insAGT GRCh37
NC_000016.8:g.16156554_16156555insAGT NCBI36
NG_007558.2:g.73275_73276insACT
NG_007558.3:g.73421_73422insACT

Transcript Alleles

HGVS Amino-acid Change
ENST00000576204.6:n.580_581insACT
ENST00000622290.5:c.*55-166_*55-165insACT ENSP00000483331.2:n.*55-166_*55-165insACT
ENST00000205557.12:c.3883-166_3883-165insACT MANE Select ENSP00000205557.7:n.3883-166_3883-165insACT
ENST00000640696.1:c.697-166_697-165insACT ENSP00000492197.1:n.697-166_697-165insACT
ENST00000205557.11:c.3883-166_3883-165insACT ENSP00000205557.7:n.3883-166_3883-165insACT
ENST00000456970.6:c.3508-166_3508-165insACT ENSP00000405002.2:n.3508-166_3508-165insACT
ENST00000576204.5:n.580_581insACT
ENST00000622290.4:c.*1092-166_*1092-165insACT ENSP00000483331.1:n.*1092-166_*1092-165insACT
NM_001171.5:c.3883-166_3883-165insACT NP_001162.4:n.3883-166_3883-165insACT
XM_011522479.1:c.3850-166_3850-165insACT XP_011520781.1:n.3850-166_3850-165insACT
XM_011522480.1:c.3541-166_3541-165insACT XP_011520782.1:n.3541-166_3541-165insACT
XM_011522481.1:c.3541-166_3541-165insACT XP_011520783.1:n.3541-166_3541-165insACT
XR_932836.1:n.4181-166_4181-165insACT
XR_932837.1:n.3919-166_3919-165insACT
XR_932838.1:n.3982-166_3982-165insACT
XR_933134.1:n.539-4585_539-4584insAGT
NM_001351800.1:c.3541-166_3541-165insACT NP_001338729.1:n.3541-166_3541-165insACT
NR_147784.1:n.3545-166_3545-165insACT
XM_011522479.2:c.3850-166_3850-165insACT XP_011520781.1:n.3850-166_3850-165insACT
XM_011522481.3:c.3541-166_3541-165insACT XP_011520783.1:n.3541-166_3541-165insACT
XM_017023212.1:c.3715-166_3715-165insACT XP_016878701.1:n.3715-166_3715-165insACT
XM_024450261.1:c.3919-166_3919-165insACT XP_024306029.1:n.3919-166_3919-165insACT
XR_932836.2:n.4127-166_4127-165insACT
XR_932837.3:n.3864-166_3864-165insACT
XR_932838.3:n.3927-166_3927-165insACT
NM_001171.6:c.3883-166_3883-165insACT MANE Select NP_001162.5:n.3883-166_3883-165insACT