Canonical Allele Identifier: CA2806038049
Gene: ABCC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.16155176_16155177insAGT , CM000678.2:g.16155176_16155177insAGT GRCh38
NC_000016.9:g.16249033_16249034insAGT , CM000678.1:g.16249033_16249034insAGT GRCh37
NC_000016.8:g.16156534_16156535insAGT NCBI36
NG_007558.2:g.73295_73296insACT
NG_007558.3:g.73441_73442insACT

Transcript Alleles

HGVS Amino-acid Change
ENST00000576204.6:n.600_601insACT
ENST00000622290.5:c.*55-146_*55-145insACT ENSP00000483331.2:n.*55-146_*55-145insACT
ENST00000205557.12:c.3883-146_3883-145insACT MANE Select ENSP00000205557.7:n.3883-146_3883-145insACT
ENST00000640696.1:c.697-146_697-145insACT ENSP00000492197.1:n.697-146_697-145insACT
ENST00000205557.11:c.3883-146_3883-145insACT ENSP00000205557.7:n.3883-146_3883-145insACT
ENST00000456970.6:c.3508-146_3508-145insACT ENSP00000405002.2:n.3508-146_3508-145insACT
ENST00000576204.5:n.600_601insACT
ENST00000622290.4:c.*1092-146_*1092-145insACT ENSP00000483331.1:n.*1092-146_*1092-145insACT
NM_001171.5:c.3883-146_3883-145insACT NP_001162.4:n.3883-146_3883-145insACT
XM_011522479.1:c.3850-146_3850-145insACT XP_011520781.1:n.3850-146_3850-145insACT
XM_011522480.1:c.3541-146_3541-145insACT XP_011520782.1:n.3541-146_3541-145insACT
XM_011522481.1:c.3541-146_3541-145insACT XP_011520783.1:n.3541-146_3541-145insACT
XR_932836.1:n.4181-146_4181-145insACT
XR_932837.1:n.3919-146_3919-145insACT
XR_932838.1:n.3982-146_3982-145insACT
XR_933134.1:n.539-4605_539-4604insAGT
NM_001351800.1:c.3541-146_3541-145insACT NP_001338729.1:n.3541-146_3541-145insACT
NR_147784.1:n.3545-146_3545-145insACT
XM_011522479.2:c.3850-146_3850-145insACT XP_011520781.1:n.3850-146_3850-145insACT
XM_011522481.3:c.3541-146_3541-145insACT XP_011520783.1:n.3541-146_3541-145insACT
XM_017023212.1:c.3715-146_3715-145insACT XP_016878701.1:n.3715-146_3715-145insACT
XM_024450261.1:c.3919-146_3919-145insACT XP_024306029.1:n.3919-146_3919-145insACT
XR_932836.2:n.4127-146_4127-145insACT
XR_932837.3:n.3864-146_3864-145insACT
XR_932838.3:n.3927-146_3927-145insACT
NM_001171.6:c.3883-146_3883-145insACT MANE Select NP_001162.5:n.3883-146_3883-145insACT