Canonical Allele Identifier: CA2806038153
Gene: ABCC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.16155282_16155283insAC , CM000678.2:g.16155282_16155283insAC GRCh38
NC_000016.9:g.16249139_16249140insAC , CM000678.1:g.16249139_16249140insAC GRCh37
NC_000016.8:g.16156640_16156641insAC NCBI36
NG_007558.2:g.73189_73190insGT
NG_007558.3:g.73335_73336insGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000576204.6:n.494_495insGT
ENST00000622290.5:c.*55-252_*55-251insGT ENSP00000483331.2:n.*55-252_*55-251insGT
ENST00000205557.12:c.3883-252_3883-251insGT MANE Select ENSP00000205557.7:n.3883-252_3883-251insGT
ENST00000640696.1:c.697-252_697-251insGT ENSP00000492197.1:n.697-252_697-251insGT
ENST00000205557.11:c.3883-252_3883-251insGT ENSP00000205557.7:n.3883-252_3883-251insGT
ENST00000456970.6:c.3508-252_3508-251insGT ENSP00000405002.2:n.3508-252_3508-251insGT
ENST00000576204.5:n.494_495insGT
ENST00000622290.4:c.*1092-252_*1092-251insGT ENSP00000483331.1:n.*1092-252_*1092-251insGT
NM_001171.5:c.3883-252_3883-251insGT NP_001162.4:n.3883-252_3883-251insGT
XM_011522479.1:c.3850-252_3850-251insGT XP_011520781.1:n.3850-252_3850-251insGT
XM_011522480.1:c.3541-252_3541-251insGT XP_011520782.1:n.3541-252_3541-251insGT
XM_011522481.1:c.3541-252_3541-251insGT XP_011520783.1:n.3541-252_3541-251insGT
XR_932836.1:n.4181-252_4181-251insGT
XR_932837.1:n.3919-252_3919-251insGT
XR_932838.1:n.3982-252_3982-251insGT
XR_933134.1:n.539-4499_539-4498insAC
NM_001351800.1:c.3541-252_3541-251insGT NP_001338729.1:n.3541-252_3541-251insGT
NR_147784.1:n.3545-252_3545-251insGT
XM_011522479.2:c.3850-252_3850-251insGT XP_011520781.1:n.3850-252_3850-251insGT
XM_011522481.3:c.3541-252_3541-251insGT XP_011520783.1:n.3541-252_3541-251insGT
XM_017023212.1:c.3715-252_3715-251insGT XP_016878701.1:n.3715-252_3715-251insGT
XM_024450261.1:c.3919-252_3919-251insGT XP_024306029.1:n.3919-252_3919-251insGT
XR_932836.2:n.4127-252_4127-251insGT
XR_932837.3:n.3864-252_3864-251insGT
XR_932838.3:n.3927-252_3927-251insGT
NM_001171.6:c.3883-252_3883-251insGT MANE Select NP_001162.5:n.3883-252_3883-251insGT