Canonical Allele Identifier: CA2210141386
Gene: ABCC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.16155329_16155331delinsATC , CM000678.2:g.16155329_16155331delinsATC GRCh38
NC_000016.9:g.16249186_16249188delinsATC , CM000678.1:g.16249186_16249188delinsATC GRCh37
NC_000016.8:g.16156687_16156689delinsATC NCBI36
NG_007558.2:g.73141_73143delinsGAT
NG_007558.3:g.73287_73289delinsGAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000576204.6:n.446_448delinsGAT
ENST00000622290.5:c.*55-300_*55-298delinsGAT ENSP00000483331.2:n.*55-300_*55-298delinsGAT
ENST00000205557.12:c.3883-300_3883-298delinsGAT MANE Select ENSP00000205557.7:n.3883-300_3883-298delinsGAT
ENST00000640696.1:c.697-300_697-298delinsGAT ENSP00000492197.1:n.697-300_697-298delinsGAT
ENST00000205557.11:c.3883-300_3883-298delinsGAT ENSP00000205557.7:n.3883-300_3883-298delinsGAT
ENST00000456970.6:c.3508-300_3508-298delinsGAT ENSP00000405002.2:n.3508-300_3508-298delinsGAT
ENST00000576204.5:n.446_448delinsGAT
ENST00000622290.4:c.*1092-300_*1092-298delinsGAT ENSP00000483331.1:n.*1092-300_*1092-298delinsGAT
NM_001171.5:c.3883-300_3883-298delinsGAT NP_001162.4:n.3883-300_3883-298delinsGAT
XM_011522479.1:c.3850-300_3850-298delinsGAT XP_011520781.1:n.3850-300_3850-298delinsGAT
XM_011522480.1:c.3541-300_3541-298delinsGAT XP_011520782.1:n.3541-300_3541-298delinsGAT
XM_011522481.1:c.3541-300_3541-298delinsGAT XP_011520783.1:n.3541-300_3541-298delinsGAT
XR_932836.1:n.4181-300_4181-298delinsGAT
XR_932837.1:n.3919-300_3919-298delinsGAT
XR_932838.1:n.3982-300_3982-298delinsGAT
XR_933134.1:n.539-4452_539-4450delinsATC
NM_001351800.1:c.3541-300_3541-298delinsGAT NP_001338729.1:n.3541-300_3541-298delinsGAT
NR_147784.1:n.3545-300_3545-298delinsGAT
XM_011522479.2:c.3850-300_3850-298delinsGAT XP_011520781.1:n.3850-300_3850-298delinsGAT
XM_011522481.3:c.3541-300_3541-298delinsGAT XP_011520783.1:n.3541-300_3541-298delinsGAT
XM_017023212.1:c.3715-300_3715-298delinsGAT XP_016878701.1:n.3715-300_3715-298delinsGAT
XM_024450261.1:c.3919-300_3919-298delinsGAT XP_024306029.1:n.3919-300_3919-298delinsGAT
XR_932836.2:n.4127-300_4127-298delinsGAT
XR_932837.3:n.3864-300_3864-298delinsGAT
XR_932838.3:n.3927-300_3927-298delinsGAT
NM_001171.6:c.3883-300_3883-298delinsGAT MANE Select NP_001162.5:n.3883-300_3883-298delinsGAT