Canonical Allele Identifier: CA2210140963
Gene: ABCC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.16154953C= , CM000678.2:g.16154953C= GRCh38
NC_000016.9:g.16248810C= , CM000678.1:g.16248810C= GRCh37
NC_000016.8:g.16156311C= NCBI36
NG_007558.2:g.73519G=
NG_007558.3:g.73665G=

Transcript Alleles

HGVS Amino-acid change
ENST00000576204.6:n.824G=
ENST00000622290.5:c.*133G= ENSP00000483331.2:n.*133G=
ENST00000205557.12:c.3961G= MANE Select ENSP00000205557.7:p.Gly1321=
ENST00000640696.1:c.775G= ENSP00000492197.1:p.Gly259=
ENST00000205557.11:c.3961G= ENSP00000205557.7:p.Gly1321=
ENST00000456970.6:c.3586G= ENSP00000405002.2:n.3586G=
ENST00000576204.5:n.824G=
ENST00000622290.4:c.*1170G= ENSP00000483331.1:n.*1170G=
NM_001171.5:c.3961G= NP_001162.4:p.Gly1321=
XM_011522479.1:c.3928G= XP_011520781.1:p.Gly1310=
XM_011522480.1:c.3619G= XP_011520782.1:p.Gly1207=
XM_011522481.1:c.3619G= XP_011520783.1:p.Gly1207=
XR_932836.1:n.4259G=
XR_932837.1:n.3997G=
XR_932838.1:n.4060G=
XR_933134.1:n.539-4828C=
NM_001351800.1:c.3619G= NP_001338729.1:p.Gly1207=
NR_147784.1:n.3623G=
XM_011522479.2:c.3928G= XP_011520781.1:p.Gly1310=
XM_011522481.3:c.3619G= XP_011520783.1:p.Gly1207=
XM_017023212.1:c.3793G= XP_016878701.1:p.Gly1265=
XM_024450261.1:c.3997G= XP_024306029.1:p.Gly1333=
XR_932837.3:n.3942G=
NM_001171.6:c.3961G= MANE Select NP_001162.5:p.Gly1321=