Canonical Allele Identifier: CA2806038101
Gene: ABCC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.16155208_16155209insACTC , CM000678.2:g.16155208_16155209insACTC GRCh38
NC_000016.9:g.16249065_16249066insACTC , CM000678.1:g.16249065_16249066insACTC GRCh37
NC_000016.8:g.16156566_16156567insACTC NCBI36
NG_007558.2:g.73263_73264insGAGT
NG_007558.3:g.73409_73410insGAGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000576204.6:n.568_569insGAGT
ENST00000622290.5:c.*55-178_*55-177insGAGT ENSP00000483331.2:n.*55-178_*55-177insGAGT
ENST00000205557.12:c.3883-178_3883-177insGAGT MANE Select ENSP00000205557.7:n.3883-178_3883-177insGAGT
ENST00000640696.1:c.697-178_697-177insGAGT ENSP00000492197.1:n.697-178_697-177insGAGT
ENST00000205557.11:c.3883-178_3883-177insGAGT ENSP00000205557.7:n.3883-178_3883-177insGAGT
ENST00000456970.6:c.3508-178_3508-177insGAGT ENSP00000405002.2:n.3508-178_3508-177insGAGT
ENST00000576204.5:n.568_569insGAGT
ENST00000622290.4:c.*1092-178_*1092-177insGAGT ENSP00000483331.1:n.*1092-178_*1092-177insGAGT
NM_001171.5:c.3883-178_3883-177insGAGT NP_001162.4:n.3883-178_3883-177insGAGT
XM_011522479.1:c.3850-178_3850-177insGAGT XP_011520781.1:n.3850-178_3850-177insGAGT
XM_011522480.1:c.3541-178_3541-177insGAGT XP_011520782.1:n.3541-178_3541-177insGAGT
XM_011522481.1:c.3541-178_3541-177insGAGT XP_011520783.1:n.3541-178_3541-177insGAGT
XR_932836.1:n.4181-178_4181-177insGAGT
XR_932837.1:n.3919-178_3919-177insGAGT
XR_932838.1:n.3982-178_3982-177insGAGT
XR_933134.1:n.539-4573_539-4572insACTC
NM_001351800.1:c.3541-178_3541-177insGAGT NP_001338729.1:n.3541-178_3541-177insGAGT
NR_147784.1:n.3545-178_3545-177insGAGT
XM_011522479.2:c.3850-178_3850-177insGAGT XP_011520781.1:n.3850-178_3850-177insGAGT
XM_011522481.3:c.3541-178_3541-177insGAGT XP_011520783.1:n.3541-178_3541-177insGAGT
XM_017023212.1:c.3715-178_3715-177insGAGT XP_016878701.1:n.3715-178_3715-177insGAGT
XM_024450261.1:c.3919-178_3919-177insGAGT XP_024306029.1:n.3919-178_3919-177insGAGT
XR_932836.2:n.4127-178_4127-177insGAGT
XR_932837.3:n.3864-178_3864-177insGAGT
XR_932838.3:n.3927-178_3927-177insGAGT
NM_001171.6:c.3883-178_3883-177insGAGT MANE Select NP_001162.5:n.3883-178_3883-177insGAGT