Canonical Allele Identifier: CA2806038030
Gene: ABCC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.16155169_16155170insACC , CM000678.2:g.16155169_16155170insACC GRCh38
NC_000016.9:g.16249026_16249027insACC , CM000678.1:g.16249026_16249027insACC GRCh37
NC_000016.8:g.16156527_16156528insACC NCBI36
NG_007558.2:g.73302_73303insGGT
NG_007558.3:g.73448_73449insGGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000576204.6:n.607_608insGGT
ENST00000622290.5:c.*55-139_*55-138insGGT ENSP00000483331.2:n.*55-139_*55-138insGGT
ENST00000205557.12:c.3883-139_3883-138insGGT MANE Select ENSP00000205557.7:n.3883-139_3883-138insGGT
ENST00000640696.1:c.697-139_697-138insGGT ENSP00000492197.1:n.697-139_697-138insGGT
ENST00000205557.11:c.3883-139_3883-138insGGT ENSP00000205557.7:n.3883-139_3883-138insGGT
ENST00000456970.6:c.3508-139_3508-138insGGT ENSP00000405002.2:n.3508-139_3508-138insGGT
ENST00000576204.5:n.607_608insGGT
ENST00000622290.4:c.*1092-139_*1092-138insGGT ENSP00000483331.1:n.*1092-139_*1092-138insGGT
NM_001171.5:c.3883-139_3883-138insGGT NP_001162.4:n.3883-139_3883-138insGGT
XM_011522479.1:c.3850-139_3850-138insGGT XP_011520781.1:n.3850-139_3850-138insGGT
XM_011522480.1:c.3541-139_3541-138insGGT XP_011520782.1:n.3541-139_3541-138insGGT
XM_011522481.1:c.3541-139_3541-138insGGT XP_011520783.1:n.3541-139_3541-138insGGT
XR_932836.1:n.4181-139_4181-138insGGT
XR_932837.1:n.3919-139_3919-138insGGT
XR_932838.1:n.3982-139_3982-138insGGT
XR_933134.1:n.539-4612_539-4611insACC
NM_001351800.1:c.3541-139_3541-138insGGT NP_001338729.1:n.3541-139_3541-138insGGT
NR_147784.1:n.3545-139_3545-138insGGT
XM_011522479.2:c.3850-139_3850-138insGGT XP_011520781.1:n.3850-139_3850-138insGGT
XM_011522481.3:c.3541-139_3541-138insGGT XP_011520783.1:n.3541-139_3541-138insGGT
XM_017023212.1:c.3715-139_3715-138insGGT XP_016878701.1:n.3715-139_3715-138insGGT
XM_024450261.1:c.3919-139_3919-138insGGT XP_024306029.1:n.3919-139_3919-138insGGT
XR_932836.2:n.4127-139_4127-138insGGT
XR_932837.3:n.3864-139_3864-138insGGT
XR_932838.3:n.3927-139_3927-138insGGT
NM_001171.6:c.3883-139_3883-138insGGT MANE Select NP_001162.5:n.3883-139_3883-138insGGT