Canonical Allele Identifier: CA2806038371
Gene: ABCC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.16198239_16198240insACTA , CM000678.2:g.16198239_16198240insACTA GRCh38
NC_000016.9:g.16292096_16292097insACTA , CM000678.1:g.16292096_16292097insACTA GRCh37
NC_000016.8:g.16199597_16199598insACTA NCBI36
NG_007558.2:g.30232_30233insTAGT
NG_007558.3:g.30378_30379insTAGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000574094.6:c.1177-58_1177-57insTAGT ENSP00000507301.1:n.1177-58_1177-57insTAGT
ENST00000622290.5:c.1177-58_1177-57insTAGT ENSP00000483331.2:n.1177-58_1177-57insTAGT
ENST00000205557.12:c.1177-58_1177-57insTAGT MANE Select ENSP00000205557.7:n.1177-58_1177-57insTAGT
ENST00000205557.11:c.1177-58_1177-57insTAGT ENSP00000205557.7:n.1177-58_1177-57insTAGT
ENST00000456970.6:c.1177-58_1177-57insTAGT ENSP00000405002.2:n.1177-58_1177-57insTAGT
ENST00000574094.5:n.1273-58_1273-57insTAGT
ENST00000622290.4:c.1177-58_1177-57insTAGT ENSP00000483331.1:n.1177-58_1177-57insTAGT
NM_001171.5:c.1177-58_1177-57insTAGT NP_001162.4:n.1177-58_1177-57insTAGT
XM_011522479.1:c.1177-58_1177-57insTAGT XP_011520781.1:n.1177-58_1177-57insTAGT
XM_011522480.1:c.835-58_835-57insTAGT XP_011520782.1:n.835-58_835-57insTAGT
XM_011522481.1:c.835-58_835-57insTAGT XP_011520783.1:n.835-58_835-57insTAGT
XM_011522482.1:c.1177-58_1177-57insTAGT XP_011520784.1:n.1177-58_1177-57insTAGT
XR_932836.1:n.1412-58_1412-57insTAGT
XR_932837.1:n.1413-58_1413-57insTAGT
XR_932838.1:n.1413-58_1413-57insTAGT
NM_001351800.1:c.835-58_835-57insTAGT NP_001338729.1:n.835-58_835-57insTAGT
NR_147784.1:n.1214-58_1214-57insTAGT
XM_011522479.2:c.1177-58_1177-57insTAGT XP_011520781.1:n.1177-58_1177-57insTAGT
XM_011522481.3:c.835-58_835-57insTAGT XP_011520783.1:n.835-58_835-57insTAGT
XM_011522482.3:c.1177-58_1177-57insTAGT XP_011520784.1:n.1177-58_1177-57insTAGT
XM_017023212.1:c.1177-58_1177-57insTAGT XP_016878701.1:n.1177-58_1177-57insTAGT
XM_017023214.1:c.1177-58_1177-57insTAGT XP_016878703.1:n.1177-58_1177-57insTAGT
XM_024450261.1:c.1213-58_1213-57insTAGT XP_024306029.1:n.1213-58_1213-57insTAGT
XR_932836.2:n.1358-58_1358-57insTAGT
XR_932837.3:n.1358-58_1358-57insTAGT
XR_932838.3:n.1358-58_1358-57insTAGT
NM_001171.6:c.1177-58_1177-57insTAGT MANE Select NP_001162.5:n.1177-58_1177-57insTAGT