Canonical Allele Identifier: CA2806038373
Gene: ABCC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.16198240_16198241insAGT , CM000678.2:g.16198240_16198241insAGT GRCh38
NC_000016.9:g.16292097_16292098insAGT , CM000678.1:g.16292097_16292098insAGT GRCh37
NC_000016.8:g.16199598_16199599insAGT NCBI36
NG_007558.2:g.30231_30232insACT
NG_007558.3:g.30377_30378insACT

Transcript Alleles

HGVS Amino-acid Change
ENST00000574094.6:c.1177-59_1177-58insACT ENSP00000507301.1:n.1177-59_1177-58insACT
ENST00000622290.5:c.1177-59_1177-58insACT ENSP00000483331.2:n.1177-59_1177-58insACT
ENST00000205557.12:c.1177-59_1177-58insACT MANE Select ENSP00000205557.7:n.1177-59_1177-58insACT
ENST00000205557.11:c.1177-59_1177-58insACT ENSP00000205557.7:n.1177-59_1177-58insACT
ENST00000456970.6:c.1177-59_1177-58insACT ENSP00000405002.2:n.1177-59_1177-58insACT
ENST00000574094.5:n.1273-59_1273-58insACT
ENST00000622290.4:c.1177-59_1177-58insACT ENSP00000483331.1:n.1177-59_1177-58insACT
NM_001171.5:c.1177-59_1177-58insACT NP_001162.4:n.1177-59_1177-58insACT
XM_011522479.1:c.1177-59_1177-58insACT XP_011520781.1:n.1177-59_1177-58insACT
XM_011522480.1:c.835-59_835-58insACT XP_011520782.1:n.835-59_835-58insACT
XM_011522481.1:c.835-59_835-58insACT XP_011520783.1:n.835-59_835-58insACT
XM_011522482.1:c.1177-59_1177-58insACT XP_011520784.1:n.1177-59_1177-58insACT
XR_932836.1:n.1412-59_1412-58insACT
XR_932837.1:n.1413-59_1413-58insACT
XR_932838.1:n.1413-59_1413-58insACT
NM_001351800.1:c.835-59_835-58insACT NP_001338729.1:n.835-59_835-58insACT
NR_147784.1:n.1214-59_1214-58insACT
XM_011522479.2:c.1177-59_1177-58insACT XP_011520781.1:n.1177-59_1177-58insACT
XM_011522481.3:c.835-59_835-58insACT XP_011520783.1:n.835-59_835-58insACT
XM_011522482.3:c.1177-59_1177-58insACT XP_011520784.1:n.1177-59_1177-58insACT
XM_017023212.1:c.1177-59_1177-58insACT XP_016878701.1:n.1177-59_1177-58insACT
XM_017023214.1:c.1177-59_1177-58insACT XP_016878703.1:n.1177-59_1177-58insACT
XM_024450261.1:c.1213-59_1213-58insACT XP_024306029.1:n.1213-59_1213-58insACT
XR_932836.2:n.1358-59_1358-58insACT
XR_932837.3:n.1358-59_1358-58insACT
XR_932838.3:n.1358-59_1358-58insACT
NM_001171.6:c.1177-59_1177-58insACT MANE Select NP_001162.5:n.1177-59_1177-58insACT