Canonical Allele Identifier: CA2806037489
Gene: ABCC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.16150916_16150917insAGT , CM000678.2:g.16150916_16150917insAGT GRCh38
NC_000016.9:g.16244773_16244774insAGT , CM000678.1:g.16244773_16244774insAGT GRCh37
NC_000016.8:g.16152274_16152275insAGT NCBI36
NG_007558.2:g.77555_77556insACT
NG_007558.3:g.77701_77702insACT

Transcript Alleles

HGVS Amino-acid Change
ENST00000622290.5:c.*381-145_*381-144insACT ENSP00000483331.2:n.*381-145_*381-144insACT
ENST00000205557.12:c.4209-145_4209-144insACT MANE Select ENSP00000205557.7:n.4209-145_4209-144insACT
ENST00000640696.1:c.1023-145_1023-144insACT ENSP00000492197.1:n.1023-145_1023-144insACT
ENST00000205557.11:c.4209-145_4209-144insACT ENSP00000205557.7:n.4209-145_4209-144insACT
ENST00000456970.6:c.3834-145_3834-144insACT ENSP00000405002.2:n.3834-145_3834-144insACT
ENST00000576204.5:n.1072-145_1072-144insACT
ENST00000622290.4:c.*1418-145_*1418-144insACT ENSP00000483331.1:n.*1418-145_*1418-144insACT
NM_001171.5:c.4209-145_4209-144insACT NP_001162.4:n.4209-145_4209-144insACT
XM_011522479.1:c.4176-145_4176-144insACT XP_011520781.1:n.4176-145_4176-144insACT
XM_011522480.1:c.3867-145_3867-144insACT XP_011520782.1:n.3867-145_3867-144insACT
XM_011522481.1:c.3867-145_3867-144insACT XP_011520783.1:n.3867-145_3867-144insACT
XR_933134.1:n.538+6626_538+6627insAGT
NM_001351800.1:c.3867-145_3867-144insACT NP_001338729.1:n.3867-145_3867-144insACT
NR_147784.1:n.3871-145_3871-144insACT
XM_011522479.2:c.4176-145_4176-144insACT XP_011520781.1:n.4176-145_4176-144insACT
XM_011522481.3:c.3867-145_3867-144insACT XP_011520783.1:n.3867-145_3867-144insACT
XM_017023212.1:c.4041-145_4041-144insACT XP_016878701.1:n.4041-145_4041-144insACT
XM_024450261.1:c.4245-145_4245-144insACT XP_024306029.1:n.4245-145_4245-144insACT
NM_001171.6:c.4209-145_4209-144insACT MANE Select NP_001162.5:n.4209-145_4209-144insACT