Canonical Allele Identifier: CA2806038383
Gene: ABCC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.16198256_16198257insA , CM000678.2:g.16198256_16198257insA GRCh38
NC_000016.9:g.16292113_16292114insA , CM000678.1:g.16292113_16292114insA GRCh37
NC_000016.8:g.16199614_16199615insA NCBI36
NG_007558.2:g.30215_30216insT
NG_007558.3:g.30361_30362insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000574094.6:c.1177-75_1177-74insT ENSP00000507301.1:n.1177-75_1177-74insT
ENST00000622290.5:c.1177-75_1177-74insT ENSP00000483331.2:n.1177-75_1177-74insT
ENST00000205557.12:c.1177-75_1177-74insT MANE Select ENSP00000205557.7:n.1177-75_1177-74insT
ENST00000205557.11:c.1177-75_1177-74insT ENSP00000205557.7:n.1177-75_1177-74insT
ENST00000456970.6:c.1177-75_1177-74insT ENSP00000405002.2:n.1177-75_1177-74insT
ENST00000574094.5:n.1273-75_1273-74insT
ENST00000622290.4:c.1177-75_1177-74insT ENSP00000483331.1:n.1177-75_1177-74insT
NM_001171.5:c.1177-75_1177-74insT NP_001162.4:n.1177-75_1177-74insT
XM_011522479.1:c.1177-75_1177-74insT XP_011520781.1:n.1177-75_1177-74insT
XM_011522480.1:c.835-75_835-74insT XP_011520782.1:n.835-75_835-74insT
XM_011522481.1:c.835-75_835-74insT XP_011520783.1:n.835-75_835-74insT
XM_011522482.1:c.1177-75_1177-74insT XP_011520784.1:n.1177-75_1177-74insT
XR_932836.1:n.1412-75_1412-74insT
XR_932837.1:n.1413-75_1413-74insT
XR_932838.1:n.1413-75_1413-74insT
NM_001351800.1:c.835-75_835-74insT NP_001338729.1:n.835-75_835-74insT
NR_147784.1:n.1214-75_1214-74insT
XM_011522479.2:c.1177-75_1177-74insT XP_011520781.1:n.1177-75_1177-74insT
XM_011522481.3:c.835-75_835-74insT XP_011520783.1:n.835-75_835-74insT
XM_011522482.3:c.1177-75_1177-74insT XP_011520784.1:n.1177-75_1177-74insT
XM_017023212.1:c.1177-75_1177-74insT XP_016878701.1:n.1177-75_1177-74insT
XM_017023214.1:c.1177-75_1177-74insT XP_016878703.1:n.1177-75_1177-74insT
XM_024450261.1:c.1213-75_1213-74insT XP_024306029.1:n.1213-75_1213-74insT
XR_932836.2:n.1358-75_1358-74insT
XR_932837.3:n.1358-75_1358-74insT
XR_932838.3:n.1358-75_1358-74insT
NM_001171.6:c.1177-75_1177-74insT MANE Select NP_001162.5:n.1177-75_1177-74insT