Canonical Allele Identifier: CA2806038381
Gene: ABCC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.16198253_16198254insAGTT , CM000678.2:g.16198253_16198254insAGTT GRCh38
NC_000016.9:g.16292110_16292111insAGTT , CM000678.1:g.16292110_16292111insAGTT GRCh37
NC_000016.8:g.16199611_16199612insAGTT NCBI36
NG_007558.2:g.30218_30219insAACT
NG_007558.3:g.30364_30365insAACT

Transcript Alleles

HGVS Amino-acid Change
ENST00000574094.6:c.1177-72_1177-71insAACT ENSP00000507301.1:n.1177-72_1177-71insAACT
ENST00000622290.5:c.1177-72_1177-71insAACT ENSP00000483331.2:n.1177-72_1177-71insAACT
ENST00000205557.12:c.1177-72_1177-71insAACT MANE Select ENSP00000205557.7:n.1177-72_1177-71insAACT
ENST00000205557.11:c.1177-72_1177-71insAACT ENSP00000205557.7:n.1177-72_1177-71insAACT
ENST00000456970.6:c.1177-72_1177-71insAACT ENSP00000405002.2:n.1177-72_1177-71insAACT
ENST00000574094.5:n.1273-72_1273-71insAACT
ENST00000622290.4:c.1177-72_1177-71insAACT ENSP00000483331.1:n.1177-72_1177-71insAACT
NM_001171.5:c.1177-72_1177-71insAACT NP_001162.4:n.1177-72_1177-71insAACT
XM_011522479.1:c.1177-72_1177-71insAACT XP_011520781.1:n.1177-72_1177-71insAACT
XM_011522480.1:c.835-72_835-71insAACT XP_011520782.1:n.835-72_835-71insAACT
XM_011522481.1:c.835-72_835-71insAACT XP_011520783.1:n.835-72_835-71insAACT
XM_011522482.1:c.1177-72_1177-71insAACT XP_011520784.1:n.1177-72_1177-71insAACT
XR_932836.1:n.1412-72_1412-71insAACT
XR_932837.1:n.1413-72_1413-71insAACT
XR_932838.1:n.1413-72_1413-71insAACT
NM_001351800.1:c.835-72_835-71insAACT NP_001338729.1:n.835-72_835-71insAACT
NR_147784.1:n.1214-72_1214-71insAACT
XM_011522479.2:c.1177-72_1177-71insAACT XP_011520781.1:n.1177-72_1177-71insAACT
XM_011522481.3:c.835-72_835-71insAACT XP_011520783.1:n.835-72_835-71insAACT
XM_011522482.3:c.1177-72_1177-71insAACT XP_011520784.1:n.1177-72_1177-71insAACT
XM_017023212.1:c.1177-72_1177-71insAACT XP_016878701.1:n.1177-72_1177-71insAACT
XM_017023214.1:c.1177-72_1177-71insAACT XP_016878703.1:n.1177-72_1177-71insAACT
XM_024450261.1:c.1213-72_1213-71insAACT XP_024306029.1:n.1213-72_1213-71insAACT
XR_932836.2:n.1358-72_1358-71insAACT
XR_932837.3:n.1358-72_1358-71insAACT
XR_932838.3:n.1358-72_1358-71insAACT
NM_001171.6:c.1177-72_1177-71insAACT MANE Select NP_001162.5:n.1177-72_1177-71insAACT