Canonical Allele Identifier: CA2806038034
Gene: ABCC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.16155170_16155171insACA , CM000678.2:g.16155170_16155171insACA GRCh38
NC_000016.9:g.16249027_16249028insACA , CM000678.1:g.16249027_16249028insACA GRCh37
NC_000016.8:g.16156528_16156529insACA NCBI36
NG_007558.2:g.73301_73302insTGT
NG_007558.3:g.73447_73448insTGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000576204.6:n.606_607insTGT
ENST00000622290.5:c.*55-140_*55-139insTGT ENSP00000483331.2:n.*55-140_*55-139insTGT
ENST00000205557.12:c.3883-140_3883-139insTGT MANE Select ENSP00000205557.7:n.3883-140_3883-139insTGT
ENST00000640696.1:c.697-140_697-139insTGT ENSP00000492197.1:n.697-140_697-139insTGT
ENST00000205557.11:c.3883-140_3883-139insTGT ENSP00000205557.7:n.3883-140_3883-139insTGT
ENST00000456970.6:c.3508-140_3508-139insTGT ENSP00000405002.2:n.3508-140_3508-139insTGT
ENST00000576204.5:n.606_607insTGT
ENST00000622290.4:c.*1092-140_*1092-139insTGT ENSP00000483331.1:n.*1092-140_*1092-139insTGT
NM_001171.5:c.3883-140_3883-139insTGT NP_001162.4:n.3883-140_3883-139insTGT
XM_011522479.1:c.3850-140_3850-139insTGT XP_011520781.1:n.3850-140_3850-139insTGT
XM_011522480.1:c.3541-140_3541-139insTGT XP_011520782.1:n.3541-140_3541-139insTGT
XM_011522481.1:c.3541-140_3541-139insTGT XP_011520783.1:n.3541-140_3541-139insTGT
XR_932836.1:n.4181-140_4181-139insTGT
XR_932837.1:n.3919-140_3919-139insTGT
XR_932838.1:n.3982-140_3982-139insTGT
XR_933134.1:n.539-4611_539-4610insACA
NM_001351800.1:c.3541-140_3541-139insTGT NP_001338729.1:n.3541-140_3541-139insTGT
NR_147784.1:n.3545-140_3545-139insTGT
XM_011522479.2:c.3850-140_3850-139insTGT XP_011520781.1:n.3850-140_3850-139insTGT
XM_011522481.3:c.3541-140_3541-139insTGT XP_011520783.1:n.3541-140_3541-139insTGT
XM_017023212.1:c.3715-140_3715-139insTGT XP_016878701.1:n.3715-140_3715-139insTGT
XM_024450261.1:c.3919-140_3919-139insTGT XP_024306029.1:n.3919-140_3919-139insTGT
XR_932836.2:n.4127-140_4127-139insTGT
XR_932837.3:n.3864-140_3864-139insTGT
XR_932838.3:n.3927-140_3927-139insTGT
NM_001171.6:c.3883-140_3883-139insTGT MANE Select NP_001162.5:n.3883-140_3883-139insTGT