Canonical Allele Identifier: CA2806038045
Gene: ABCC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.16155174_16155175insAG , CM000678.2:g.16155174_16155175insAG GRCh38
NC_000016.9:g.16249031_16249032insAG , CM000678.1:g.16249031_16249032insAG GRCh37
NC_000016.8:g.16156532_16156533insAG NCBI36
NG_007558.2:g.73297_73298insCT
NG_007558.3:g.73443_73444insCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000576204.6:n.602_603insCT
ENST00000622290.5:c.*55-144_*55-143insCT ENSP00000483331.2:n.*55-144_*55-143insCT
ENST00000205557.12:c.3883-144_3883-143insCT MANE Select ENSP00000205557.7:n.3883-144_3883-143insCT
ENST00000640696.1:c.697-144_697-143insCT ENSP00000492197.1:n.697-144_697-143insCT
ENST00000205557.11:c.3883-144_3883-143insCT ENSP00000205557.7:n.3883-144_3883-143insCT
ENST00000456970.6:c.3508-144_3508-143insCT ENSP00000405002.2:n.3508-144_3508-143insCT
ENST00000576204.5:n.602_603insCT
ENST00000622290.4:c.*1092-144_*1092-143insCT ENSP00000483331.1:n.*1092-144_*1092-143insCT
NM_001171.5:c.3883-144_3883-143insCT NP_001162.4:n.3883-144_3883-143insCT
XM_011522479.1:c.3850-144_3850-143insCT XP_011520781.1:n.3850-144_3850-143insCT
XM_011522480.1:c.3541-144_3541-143insCT XP_011520782.1:n.3541-144_3541-143insCT
XM_011522481.1:c.3541-144_3541-143insCT XP_011520783.1:n.3541-144_3541-143insCT
XR_932836.1:n.4181-144_4181-143insCT
XR_932837.1:n.3919-144_3919-143insCT
XR_932838.1:n.3982-144_3982-143insCT
XR_933134.1:n.539-4607_539-4606insAG
NM_001351800.1:c.3541-144_3541-143insCT NP_001338729.1:n.3541-144_3541-143insCT
NR_147784.1:n.3545-144_3545-143insCT
XM_011522479.2:c.3850-144_3850-143insCT XP_011520781.1:n.3850-144_3850-143insCT
XM_011522481.3:c.3541-144_3541-143insCT XP_011520783.1:n.3541-144_3541-143insCT
XM_017023212.1:c.3715-144_3715-143insCT XP_016878701.1:n.3715-144_3715-143insCT
XM_024450261.1:c.3919-144_3919-143insCT XP_024306029.1:n.3919-144_3919-143insCT
XR_932836.2:n.4127-144_4127-143insCT
XR_932837.3:n.3864-144_3864-143insCT
XR_932838.3:n.3927-144_3927-143insCT
NM_001171.6:c.3883-144_3883-143insCT MANE Select NP_001162.5:n.3883-144_3883-143insCT