Canonical Allele Identifier: CA2806038142
Gene: ABCC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.16155243_16155244insAGT , CM000678.2:g.16155243_16155244insAGT GRCh38
NC_000016.9:g.16249100_16249101insAGT , CM000678.1:g.16249100_16249101insAGT GRCh37
NC_000016.8:g.16156601_16156602insAGT NCBI36
NG_007558.2:g.73228_73229insACT
NG_007558.3:g.73374_73375insACT

Transcript Alleles

HGVS Amino-acid Change
ENST00000576204.6:n.533_534insACT
ENST00000622290.5:c.*55-213_*55-212insACT ENSP00000483331.2:n.*55-213_*55-212insACT
ENST00000205557.12:c.3883-213_3883-212insACT MANE Select ENSP00000205557.7:n.3883-213_3883-212insACT
ENST00000640696.1:c.697-213_697-212insACT ENSP00000492197.1:n.697-213_697-212insACT
ENST00000205557.11:c.3883-213_3883-212insACT ENSP00000205557.7:n.3883-213_3883-212insACT
ENST00000456970.6:c.3508-213_3508-212insACT ENSP00000405002.2:n.3508-213_3508-212insACT
ENST00000576204.5:n.533_534insACT
ENST00000622290.4:c.*1092-213_*1092-212insACT ENSP00000483331.1:n.*1092-213_*1092-212insACT
NM_001171.5:c.3883-213_3883-212insACT NP_001162.4:n.3883-213_3883-212insACT
XM_011522479.1:c.3850-213_3850-212insACT XP_011520781.1:n.3850-213_3850-212insACT
XM_011522480.1:c.3541-213_3541-212insACT XP_011520782.1:n.3541-213_3541-212insACT
XM_011522481.1:c.3541-213_3541-212insACT XP_011520783.1:n.3541-213_3541-212insACT
XR_932836.1:n.4181-213_4181-212insACT
XR_932837.1:n.3919-213_3919-212insACT
XR_932838.1:n.3982-213_3982-212insACT
XR_933134.1:n.539-4538_539-4537insAGT
NM_001351800.1:c.3541-213_3541-212insACT NP_001338729.1:n.3541-213_3541-212insACT
NR_147784.1:n.3545-213_3545-212insACT
XM_011522479.2:c.3850-213_3850-212insACT XP_011520781.1:n.3850-213_3850-212insACT
XM_011522481.3:c.3541-213_3541-212insACT XP_011520783.1:n.3541-213_3541-212insACT
XM_017023212.1:c.3715-213_3715-212insACT XP_016878701.1:n.3715-213_3715-212insACT
XM_024450261.1:c.3919-213_3919-212insACT XP_024306029.1:n.3919-213_3919-212insACT
XR_932836.2:n.4127-213_4127-212insACT
XR_932837.3:n.3864-213_3864-212insACT
XR_932838.3:n.3927-213_3927-212insACT
NM_001171.6:c.3883-213_3883-212insACT MANE Select NP_001162.5:n.3883-213_3883-212insACT