Canonical Allele Identifier: CA2806037808
Gene: ABCC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.16163249_16163250insACA , CM000678.2:g.16163249_16163250insACA GRCh38
NC_000016.9:g.16257106_16257107insACA , CM000678.1:g.16257106_16257107insACA GRCh37
NC_000016.8:g.16164607_16164608insACA NCBI36
NG_007558.2:g.65222_65223insTGT
NG_007558.3:g.65368_65369insTGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000622290.5:c.3307-58_3307-57insTGT ENSP00000483331.2:n.3307-58_3307-57insTGT
ENST00000205557.12:c.3307-58_3307-57insTGT MANE Select ENSP00000205557.7:n.3307-58_3307-57insTGT
ENST00000640696.1:c.321-1686_321-1685insTGT ENSP00000492197.1:n.321-1686_321-1685insTGT
ENST00000205557.11:c.3307-58_3307-57insTGT ENSP00000205557.7:n.3307-58_3307-57insTGT
ENST00000456970.6:c.3132-1686_3132-1685insTGT ENSP00000405002.2:n.3132-1686_3132-1685insTGT
ENST00000622290.4:c.*516-58_*516-57insTGT ENSP00000483331.1:n.*516-58_*516-57insTGT
NM_001171.5:c.3307-58_3307-57insTGT NP_001162.4:n.3307-58_3307-57insTGT
XM_011522479.1:c.3274-58_3274-57insTGT XP_011520781.1:n.3274-58_3274-57insTGT
XM_011522480.1:c.2965-58_2965-57insTGT XP_011520782.1:n.2965-58_2965-57insTGT
XM_011522481.1:c.2965-58_2965-57insTGT XP_011520783.1:n.2965-58_2965-57insTGT
XR_932836.1:n.3542-58_3542-57insTGT
XR_932837.1:n.3543-1686_3543-1685insTGT
XR_932838.1:n.3543-1686_3543-1685insTGT
XR_933133.1:n.407+406_407+407insACA
XR_933134.1:n.754+406_754+407insACA
NM_001351800.1:c.2965-58_2965-57insTGT NP_001338729.1:n.2965-58_2965-57insTGT
NR_147784.1:n.3169-1686_3169-1685insTGT
XM_011522479.2:c.3274-58_3274-57insTGT XP_011520781.1:n.3274-58_3274-57insTGT
XM_011522481.3:c.2965-58_2965-57insTGT XP_011520783.1:n.2965-58_2965-57insTGT
XM_017023212.1:c.3139-58_3139-57insTGT XP_016878701.1:n.3139-58_3139-57insTGT
XM_017023214.1:c.3307-1686_3307-1685insTGT XP_016878703.1:n.3307-1686_3307-1685insTGT
XM_024450261.1:c.3343-58_3343-57insTGT XP_024306029.1:n.3343-58_3343-57insTGT
XR_932836.2:n.3488-58_3488-57insTGT
XR_932837.3:n.3488-1686_3488-1685insTGT
XR_932838.3:n.3488-1686_3488-1685insTGT
NM_001171.6:c.3307-58_3307-57insTGT MANE Select NP_001162.5:n.3307-58_3307-57insTGT