Canonical Allele Identifier: CA2210140966
Gene: ABCC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.16154956C= , CM000678.2:g.16154956C= GRCh38
NC_000016.9:g.16248813C= , CM000678.1:g.16248813C= GRCh37
NC_000016.8:g.16156314C= NCBI36
NG_007558.2:g.73516G=
NG_007558.3:g.73662G=

Transcript Alleles

HGVS Amino-acid change
ENST00000576204.6:n.821G=
ENST00000622290.5:c.*130G= ENSP00000483331.2:n.*130G=
ENST00000205557.12:c.3958G= MANE Select ENSP00000205557.7:p.Glu1320=
ENST00000640696.1:c.772G= ENSP00000492197.1:p.Glu258=
ENST00000205557.11:c.3958G= ENSP00000205557.7:p.Glu1320=
ENST00000456970.6:c.3583G= ENSP00000405002.2:n.3583G=
ENST00000576204.5:n.821G=
ENST00000622290.4:c.*1167G= ENSP00000483331.1:n.*1167G=
NM_001171.5:c.3958G= NP_001162.4:p.Glu1320=
XM_011522479.1:c.3925G= XP_011520781.1:p.Glu1309=
XM_011522480.1:c.3616G= XP_011520782.1:p.Glu1206=
XM_011522481.1:c.3616G= XP_011520783.1:p.Glu1206=
XR_932836.1:n.4256G=
XR_932837.1:n.3994G=
XR_932838.1:n.4057G=
XR_933134.1:n.539-4825C=
NM_001351800.1:c.3616G= NP_001338729.1:p.Glu1206=
NR_147784.1:n.3620G=
XM_011522479.2:c.3925G= XP_011520781.1:p.Glu1309=
XM_011522481.3:c.3616G= XP_011520783.1:p.Glu1206=
XM_017023212.1:c.3790G= XP_016878701.1:p.Glu1264=
XM_024450261.1:c.3994G= XP_024306029.1:p.Glu1332=
XR_932837.3:n.3939G=
NM_001171.6:c.3958G= MANE Select NP_001162.5:p.Glu1320=