Canonical Allele Identifier: CA2806038074
Gene: ABCC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.16155188_16155189insAGG , CM000678.2:g.16155188_16155189insAGG GRCh38
NC_000016.9:g.16249045_16249046insAGG , CM000678.1:g.16249045_16249046insAGG GRCh37
NC_000016.8:g.16156546_16156547insAGG NCBI36
NG_007558.2:g.73283_73284insCCT
NG_007558.3:g.73429_73430insCCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000576204.6:n.588_589insCCT
ENST00000622290.5:c.*55-158_*55-157insCCT ENSP00000483331.2:n.*55-158_*55-157insCCT
ENST00000205557.12:c.3883-158_3883-157insCCT MANE Select ENSP00000205557.7:n.3883-158_3883-157insCCT
ENST00000640696.1:c.697-158_697-157insCCT ENSP00000492197.1:n.697-158_697-157insCCT
ENST00000205557.11:c.3883-158_3883-157insCCT ENSP00000205557.7:n.3883-158_3883-157insCCT
ENST00000456970.6:c.3508-158_3508-157insCCT ENSP00000405002.2:n.3508-158_3508-157insCCT
ENST00000576204.5:n.588_589insCCT
ENST00000622290.4:c.*1092-158_*1092-157insCCT ENSP00000483331.1:n.*1092-158_*1092-157insCCT
NM_001171.5:c.3883-158_3883-157insCCT NP_001162.4:n.3883-158_3883-157insCCT
XM_011522479.1:c.3850-158_3850-157insCCT XP_011520781.1:n.3850-158_3850-157insCCT
XM_011522480.1:c.3541-158_3541-157insCCT XP_011520782.1:n.3541-158_3541-157insCCT
XM_011522481.1:c.3541-158_3541-157insCCT XP_011520783.1:n.3541-158_3541-157insCCT
XR_932836.1:n.4181-158_4181-157insCCT
XR_932837.1:n.3919-158_3919-157insCCT
XR_932838.1:n.3982-158_3982-157insCCT
XR_933134.1:n.539-4593_539-4592insAGG
NM_001351800.1:c.3541-158_3541-157insCCT NP_001338729.1:n.3541-158_3541-157insCCT
NR_147784.1:n.3545-158_3545-157insCCT
XM_011522479.2:c.3850-158_3850-157insCCT XP_011520781.1:n.3850-158_3850-157insCCT
XM_011522481.3:c.3541-158_3541-157insCCT XP_011520783.1:n.3541-158_3541-157insCCT
XM_017023212.1:c.3715-158_3715-157insCCT XP_016878701.1:n.3715-158_3715-157insCCT
XM_024450261.1:c.3919-158_3919-157insCCT XP_024306029.1:n.3919-158_3919-157insCCT
XR_932836.2:n.4127-158_4127-157insCCT
XR_932837.3:n.3864-158_3864-157insCCT
XR_932838.3:n.3927-158_3927-157insCCT
NM_001171.6:c.3883-158_3883-157insCCT MANE Select NP_001162.5:n.3883-158_3883-157insCCT