Canonical Allele Identifier: CA2806038036
Gene: ABCC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.16155171_16155172insACA , CM000678.2:g.16155171_16155172insACA GRCh38
NC_000016.9:g.16249028_16249029insACA , CM000678.1:g.16249028_16249029insACA GRCh37
NC_000016.8:g.16156529_16156530insACA NCBI36
NG_007558.2:g.73300_73301insTGT
NG_007558.3:g.73446_73447insTGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000576204.6:n.605_606insTGT
ENST00000622290.5:c.*55-141_*55-140insTGT ENSP00000483331.2:n.*55-141_*55-140insTGT
ENST00000205557.12:c.3883-141_3883-140insTGT MANE Select ENSP00000205557.7:n.3883-141_3883-140insTGT
ENST00000640696.1:c.697-141_697-140insTGT ENSP00000492197.1:n.697-141_697-140insTGT
ENST00000205557.11:c.3883-141_3883-140insTGT ENSP00000205557.7:n.3883-141_3883-140insTGT
ENST00000456970.6:c.3508-141_3508-140insTGT ENSP00000405002.2:n.3508-141_3508-140insTGT
ENST00000576204.5:n.605_606insTGT
ENST00000622290.4:c.*1092-141_*1092-140insTGT ENSP00000483331.1:n.*1092-141_*1092-140insTGT
NM_001171.5:c.3883-141_3883-140insTGT NP_001162.4:n.3883-141_3883-140insTGT
XM_011522479.1:c.3850-141_3850-140insTGT XP_011520781.1:n.3850-141_3850-140insTGT
XM_011522480.1:c.3541-141_3541-140insTGT XP_011520782.1:n.3541-141_3541-140insTGT
XM_011522481.1:c.3541-141_3541-140insTGT XP_011520783.1:n.3541-141_3541-140insTGT
XR_932836.1:n.4181-141_4181-140insTGT
XR_932837.1:n.3919-141_3919-140insTGT
XR_932838.1:n.3982-141_3982-140insTGT
XR_933134.1:n.539-4610_539-4609insACA
NM_001351800.1:c.3541-141_3541-140insTGT NP_001338729.1:n.3541-141_3541-140insTGT
NR_147784.1:n.3545-141_3545-140insTGT
XM_011522479.2:c.3850-141_3850-140insTGT XP_011520781.1:n.3850-141_3850-140insTGT
XM_011522481.3:c.3541-141_3541-140insTGT XP_011520783.1:n.3541-141_3541-140insTGT
XM_017023212.1:c.3715-141_3715-140insTGT XP_016878701.1:n.3715-141_3715-140insTGT
XM_024450261.1:c.3919-141_3919-140insTGT XP_024306029.1:n.3919-141_3919-140insTGT
XR_932836.2:n.4127-141_4127-140insTGT
XR_932837.3:n.3864-141_3864-140insTGT
XR_932838.3:n.3927-141_3927-140insTGT
NM_001171.6:c.3883-141_3883-140insTGT MANE Select NP_001162.5:n.3883-141_3883-140insTGT