Canonical Allele Identifier: CA2210131827
Gene: ABCC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.16159508G= , CM000678.2:g.16159508G= GRCh38
NC_000016.9:g.16253365G= , CM000678.1:g.16253365G= GRCh37
NC_000016.8:g.16160866G= NCBI36
NG_007558.2:g.68964C=
NG_007558.3:g.69110C=

Transcript Alleles

HGVS Amino-acid change
ENST00000622290.5:c.3709C= ENSP00000483331.2:p.Gln1237=
ENST00000205557.12:c.3709C= MANE Select ENSP00000205557.7:p.Gln1237=
ENST00000640696.1:c.523C= ENSP00000492197.1:p.Gln175=
ENST00000205557.11:c.3709C= ENSP00000205557.7:p.Gln1237=
ENST00000456970.6:c.3334C= ENSP00000405002.2:n.3334C=
ENST00000622290.4:c.*918C= ENSP00000483331.1:n.*918C=
NM_001171.5:c.3709C= NP_001162.4:p.Gln1237=
XM_011522479.1:c.3676C= XP_011520781.1:p.Gln1226=
XM_011522480.1:c.3367C= XP_011520782.1:p.Gln1123=
XM_011522481.1:c.3367C= XP_011520783.1:p.Gln1123=
XR_932836.1:n.3944C=
XR_932837.1:n.3745C=
XR_932838.1:n.3745C=
XR_933134.1:n.539-273G=
NM_001351800.1:c.3367C= NP_001338729.1:p.Gln1123=
NR_147784.1:n.3371C=
XM_011522479.2:c.3676C= XP_011520781.1:p.Gln1226=
XM_011522481.3:c.3367C= XP_011520783.1:p.Gln1123=
XM_017023212.1:c.3541C= XP_016878701.1:p.Gln1181=
XM_024450261.1:c.3745C= XP_024306029.1:p.Gln1249=
XR_932836.2:n.3890C=
XR_932837.3:n.3690C=
XR_932838.3:n.3690C=
NM_001171.6:c.3709C= MANE Select NP_001162.5:p.Gln1237=