Canonical Allele Identifier: CA2806038140
Gene: ABCC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.16155241_16155242insAC , CM000678.2:g.16155241_16155242insAC GRCh38
NC_000016.9:g.16249098_16249099insAC , CM000678.1:g.16249098_16249099insAC GRCh37
NC_000016.8:g.16156599_16156600insAC NCBI36
NG_007558.2:g.73230_73231insGT
NG_007558.3:g.73376_73377insGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000576204.6:n.535_536insGT
ENST00000622290.5:c.*55-211_*55-210insGT ENSP00000483331.2:n.*55-211_*55-210insGT
ENST00000205557.12:c.3883-211_3883-210insGT MANE Select ENSP00000205557.7:n.3883-211_3883-210insGT
ENST00000640696.1:c.697-211_697-210insGT ENSP00000492197.1:n.697-211_697-210insGT
ENST00000205557.11:c.3883-211_3883-210insGT ENSP00000205557.7:n.3883-211_3883-210insGT
ENST00000456970.6:c.3508-211_3508-210insGT ENSP00000405002.2:n.3508-211_3508-210insGT
ENST00000576204.5:n.535_536insGT
ENST00000622290.4:c.*1092-211_*1092-210insGT ENSP00000483331.1:n.*1092-211_*1092-210insGT
NM_001171.5:c.3883-211_3883-210insGT NP_001162.4:n.3883-211_3883-210insGT
XM_011522479.1:c.3850-211_3850-210insGT XP_011520781.1:n.3850-211_3850-210insGT
XM_011522480.1:c.3541-211_3541-210insGT XP_011520782.1:n.3541-211_3541-210insGT
XM_011522481.1:c.3541-211_3541-210insGT XP_011520783.1:n.3541-211_3541-210insGT
XR_932836.1:n.4181-211_4181-210insGT
XR_932837.1:n.3919-211_3919-210insGT
XR_932838.1:n.3982-211_3982-210insGT
XR_933134.1:n.539-4540_539-4539insAC
NM_001351800.1:c.3541-211_3541-210insGT NP_001338729.1:n.3541-211_3541-210insGT
NR_147784.1:n.3545-211_3545-210insGT
XM_011522479.2:c.3850-211_3850-210insGT XP_011520781.1:n.3850-211_3850-210insGT
XM_011522481.3:c.3541-211_3541-210insGT XP_011520783.1:n.3541-211_3541-210insGT
XM_017023212.1:c.3715-211_3715-210insGT XP_016878701.1:n.3715-211_3715-210insGT
XM_024450261.1:c.3919-211_3919-210insGT XP_024306029.1:n.3919-211_3919-210insGT
XR_932836.2:n.4127-211_4127-210insGT
XR_932837.3:n.3864-211_3864-210insGT
XR_932838.3:n.3927-211_3927-210insGT
NM_001171.6:c.3883-211_3883-210insGT MANE Select NP_001162.5:n.3883-211_3883-210insGT