Canonical Allele Identifier: CA2806038023
Gene: ABCC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.16155168_16155169insAGT , CM000678.2:g.16155168_16155169insAGT GRCh38
NC_000016.9:g.16249025_16249026insAGT , CM000678.1:g.16249025_16249026insAGT GRCh37
NC_000016.8:g.16156526_16156527insAGT NCBI36
NG_007558.2:g.73303_73304insACT
NG_007558.3:g.73449_73450insACT

Transcript Alleles

HGVS Amino-acid Change
ENST00000576204.6:n.608_609insACT
ENST00000622290.5:c.*55-138_*55-137insACT ENSP00000483331.2:n.*55-138_*55-137insACT
ENST00000205557.12:c.3883-138_3883-137insACT MANE Select ENSP00000205557.7:n.3883-138_3883-137insACT
ENST00000640696.1:c.697-138_697-137insACT ENSP00000492197.1:n.697-138_697-137insACT
ENST00000205557.11:c.3883-138_3883-137insACT ENSP00000205557.7:n.3883-138_3883-137insACT
ENST00000456970.6:c.3508-138_3508-137insACT ENSP00000405002.2:n.3508-138_3508-137insACT
ENST00000576204.5:n.608_609insACT
ENST00000622290.4:c.*1092-138_*1092-137insACT ENSP00000483331.1:n.*1092-138_*1092-137insACT
NM_001171.5:c.3883-138_3883-137insACT NP_001162.4:n.3883-138_3883-137insACT
XM_011522479.1:c.3850-138_3850-137insACT XP_011520781.1:n.3850-138_3850-137insACT
XM_011522480.1:c.3541-138_3541-137insACT XP_011520782.1:n.3541-138_3541-137insACT
XM_011522481.1:c.3541-138_3541-137insACT XP_011520783.1:n.3541-138_3541-137insACT
XR_932836.1:n.4181-138_4181-137insACT
XR_932837.1:n.3919-138_3919-137insACT
XR_932838.1:n.3982-138_3982-137insACT
XR_933134.1:n.539-4613_539-4612insAGT
NM_001351800.1:c.3541-138_3541-137insACT NP_001338729.1:n.3541-138_3541-137insACT
NR_147784.1:n.3545-138_3545-137insACT
XM_011522479.2:c.3850-138_3850-137insACT XP_011520781.1:n.3850-138_3850-137insACT
XM_011522481.3:c.3541-138_3541-137insACT XP_011520783.1:n.3541-138_3541-137insACT
XM_017023212.1:c.3715-138_3715-137insACT XP_016878701.1:n.3715-138_3715-137insACT
XM_024450261.1:c.3919-138_3919-137insACT XP_024306029.1:n.3919-138_3919-137insACT
XR_932836.2:n.4127-138_4127-137insACT
XR_932837.3:n.3864-138_3864-137insACT
XR_932838.3:n.3927-138_3927-137insACT
NM_001171.6:c.3883-138_3883-137insACT MANE Select NP_001162.5:n.3883-138_3883-137insACT