Canonical Allele Identifier: CA2210140959
Gene: ABCC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.16154949C= , CM000678.2:g.16154949C= GRCh38
NC_000016.9:g.16248806C= , CM000678.1:g.16248806C= GRCh37
NC_000016.8:g.16156307C= NCBI36
NG_007558.2:g.73523G=
NG_007558.3:g.73669G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000576204.6:n.828G=
ENST00000622290.5:c.*137G= ENSP00000483331.2:n.*137G=
ENST00000205557.12:c.3965G= MANE Select ENSP00000205557.7:p.Gly1322=
ENST00000640696.1:c.779G= ENSP00000492197.1:p.Gly260=
ENST00000205557.11:c.3965G= ENSP00000205557.7:p.Gly1322=
ENST00000456970.6:c.3590G= ENSP00000405002.2:n.3590G=
ENST00000576204.5:n.828G=
ENST00000622290.4:c.*1174G= ENSP00000483331.1:n.*1174G=
NM_001171.5:c.3965G= NP_001162.4:p.Gly1322=
XM_011522479.1:c.3932G= XP_011520781.1:p.Gly1311=
XM_011522480.1:c.3623G= XP_011520782.1:p.Gly1208=
XM_011522481.1:c.3623G= XP_011520783.1:p.Gly1208=
XR_932836.1:n.4263G=
XR_932837.1:n.4001G=
XR_932838.1:n.4064G=
XR_933134.1:n.539-4832C=
NM_001351800.1:c.3623G= NP_001338729.1:p.Gly1208=
NR_147784.1:n.3627G=
XM_011522479.2:c.3932G= XP_011520781.1:p.Gly1311=
XM_011522481.3:c.3623G= XP_011520783.1:p.Gly1208=
XM_017023212.1:c.3797G= XP_016878701.1:p.Gly1266=
XM_024450261.1:c.4001G= XP_024306029.1:p.Gly1334=
XR_932837.3:n.3946G=
NM_001171.6:c.3965G= MANE Select NP_001162.5:p.Gly1322=