Canonical Allele Identifier: CA2210135551
Gene: ABCC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.16150830_16150832delinsTGG , CM000678.2:g.16150830_16150832delinsTGG GRCh38
NC_000016.9:g.16244687_16244689delinsTGG , CM000678.1:g.16244687_16244689delinsTGG GRCh37
NC_000016.8:g.16152188_16152190delinsTGG NCBI36
NG_007558.2:g.77640_77642delinsCCA
NG_007558.3:g.77786_77788delinsCCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000622290.5:c.*381-60_*381-58delinsCCA ENSP00000483331.2:n.*381-60_*381-58delinsCCA
ENST00000205557.12:c.4209-60_4209-58delinsCCA MANE Select ENSP00000205557.7:n.4209-60_4209-58delinsCCA
ENST00000640696.1:c.1023-60_1023-58delinsCCA ENSP00000492197.1:n.1023-60_1023-58delinsCCA
ENST00000205557.11:c.4209-60_4209-58delinsCCA ENSP00000205557.7:n.4209-60_4209-58delinsCCA
ENST00000456970.6:c.3834-60_3834-58delinsCCA ENSP00000405002.2:n.3834-60_3834-58delinsCCA
ENST00000576204.5:n.1072-60_1072-58delinsCCA
ENST00000622290.4:c.*1418-60_*1418-58delinsCCA ENSP00000483331.1:n.*1418-60_*1418-58delinsCCA
NM_001171.5:c.4209-60_4209-58delinsCCA NP_001162.4:n.4209-60_4209-58delinsCCA
XM_011522479.1:c.4176-60_4176-58delinsCCA XP_011520781.1:n.4176-60_4176-58delinsCCA
XM_011522480.1:c.3867-60_3867-58delinsCCA XP_011520782.1:n.3867-60_3867-58delinsCCA
XM_011522481.1:c.3867-60_3867-58delinsCCA XP_011520783.1:n.3867-60_3867-58delinsCCA
XR_933134.1:n.538+6540_538+6542delinsTGG
NM_001351800.1:c.3867-60_3867-58delinsCCA NP_001338729.1:n.3867-60_3867-58delinsCCA
NR_147784.1:n.3871-60_3871-58delinsCCA
XM_011522479.2:c.4176-60_4176-58delinsCCA XP_011520781.1:n.4176-60_4176-58delinsCCA
XM_011522481.3:c.3867-60_3867-58delinsCCA XP_011520783.1:n.3867-60_3867-58delinsCCA
XM_017023212.1:c.4041-60_4041-58delinsCCA XP_016878701.1:n.4041-60_4041-58delinsCCA
XM_024450261.1:c.4245-60_4245-58delinsCCA XP_024306029.1:n.4245-60_4245-58delinsCCA
NM_001171.6:c.4209-60_4209-58delinsCCA MANE Select NP_001162.5:n.4209-60_4209-58delinsCCA