Canonical Allele Identifier: CA2806038127
Gene: ABCC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.16155230_16155231insAG , CM000678.2:g.16155230_16155231insAG GRCh38
NC_000016.9:g.16249087_16249088insAG , CM000678.1:g.16249087_16249088insAG GRCh37
NC_000016.8:g.16156588_16156589insAG NCBI36
NG_007558.2:g.73241_73242insCT
NG_007558.3:g.73387_73388insCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000576204.6:n.546_547insCT
ENST00000622290.5:c.*55-200_*55-199insCT ENSP00000483331.2:n.*55-200_*55-199insCT
ENST00000205557.12:c.3883-200_3883-199insCT MANE Select ENSP00000205557.7:n.3883-200_3883-199insCT
ENST00000640696.1:c.697-200_697-199insCT ENSP00000492197.1:n.697-200_697-199insCT
ENST00000205557.11:c.3883-200_3883-199insCT ENSP00000205557.7:n.3883-200_3883-199insCT
ENST00000456970.6:c.3508-200_3508-199insCT ENSP00000405002.2:n.3508-200_3508-199insCT
ENST00000576204.5:n.546_547insCT
ENST00000622290.4:c.*1092-200_*1092-199insCT ENSP00000483331.1:n.*1092-200_*1092-199insCT
NM_001171.5:c.3883-200_3883-199insCT NP_001162.4:n.3883-200_3883-199insCT
XM_011522479.1:c.3850-200_3850-199insCT XP_011520781.1:n.3850-200_3850-199insCT
XM_011522480.1:c.3541-200_3541-199insCT XP_011520782.1:n.3541-200_3541-199insCT
XM_011522481.1:c.3541-200_3541-199insCT XP_011520783.1:n.3541-200_3541-199insCT
XR_932836.1:n.4181-200_4181-199insCT
XR_932837.1:n.3919-200_3919-199insCT
XR_932838.1:n.3982-200_3982-199insCT
XR_933134.1:n.539-4551_539-4550insAG
NM_001351800.1:c.3541-200_3541-199insCT NP_001338729.1:n.3541-200_3541-199insCT
NR_147784.1:n.3545-200_3545-199insCT
XM_011522479.2:c.3850-200_3850-199insCT XP_011520781.1:n.3850-200_3850-199insCT
XM_011522481.3:c.3541-200_3541-199insCT XP_011520783.1:n.3541-200_3541-199insCT
XM_017023212.1:c.3715-200_3715-199insCT XP_016878701.1:n.3715-200_3715-199insCT
XM_024450261.1:c.3919-200_3919-199insCT XP_024306029.1:n.3919-200_3919-199insCT
XR_932836.2:n.4127-200_4127-199insCT
XR_932837.3:n.3864-200_3864-199insCT
XR_932838.3:n.3927-200_3927-199insCT
NM_001171.6:c.3883-200_3883-199insCT MANE Select NP_001162.5:n.3883-200_3883-199insCT