Canonical Allele Identifier: CA2806038130
Gene: ABCC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.16155232_16155233insAG , CM000678.2:g.16155232_16155233insAG GRCh38
NC_000016.9:g.16249089_16249090insAG , CM000678.1:g.16249089_16249090insAG GRCh37
NC_000016.8:g.16156590_16156591insAG NCBI36
NG_007558.2:g.73239_73240insCT
NG_007558.3:g.73385_73386insCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000576204.6:n.544_545insCT
ENST00000622290.5:c.*55-202_*55-201insCT ENSP00000483331.2:n.*55-202_*55-201insCT
ENST00000205557.12:c.3883-202_3883-201insCT MANE Select ENSP00000205557.7:n.3883-202_3883-201insCT
ENST00000640696.1:c.697-202_697-201insCT ENSP00000492197.1:n.697-202_697-201insCT
ENST00000205557.11:c.3883-202_3883-201insCT ENSP00000205557.7:n.3883-202_3883-201insCT
ENST00000456970.6:c.3508-202_3508-201insCT ENSP00000405002.2:n.3508-202_3508-201insCT
ENST00000576204.5:n.544_545insCT
ENST00000622290.4:c.*1092-202_*1092-201insCT ENSP00000483331.1:n.*1092-202_*1092-201insCT
NM_001171.5:c.3883-202_3883-201insCT NP_001162.4:n.3883-202_3883-201insCT
XM_011522479.1:c.3850-202_3850-201insCT XP_011520781.1:n.3850-202_3850-201insCT
XM_011522480.1:c.3541-202_3541-201insCT XP_011520782.1:n.3541-202_3541-201insCT
XM_011522481.1:c.3541-202_3541-201insCT XP_011520783.1:n.3541-202_3541-201insCT
XR_932836.1:n.4181-202_4181-201insCT
XR_932837.1:n.3919-202_3919-201insCT
XR_932838.1:n.3982-202_3982-201insCT
XR_933134.1:n.539-4549_539-4548insAG
NM_001351800.1:c.3541-202_3541-201insCT NP_001338729.1:n.3541-202_3541-201insCT
NR_147784.1:n.3545-202_3545-201insCT
XM_011522479.2:c.3850-202_3850-201insCT XP_011520781.1:n.3850-202_3850-201insCT
XM_011522481.3:c.3541-202_3541-201insCT XP_011520783.1:n.3541-202_3541-201insCT
XM_017023212.1:c.3715-202_3715-201insCT XP_016878701.1:n.3715-202_3715-201insCT
XM_024450261.1:c.3919-202_3919-201insCT XP_024306029.1:n.3919-202_3919-201insCT
XR_932836.2:n.4127-202_4127-201insCT
XR_932837.3:n.3864-202_3864-201insCT
XR_932838.3:n.3927-202_3927-201insCT
NM_001171.6:c.3883-202_3883-201insCT MANE Select NP_001162.5:n.3883-202_3883-201insCT