Canonical Allele Identifier: CA2210132006
Gene: ABCC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.16159556G= , CM000678.2:g.16159556G= GRCh38
NC_000016.9:g.16253413G= , CM000678.1:g.16253413G= GRCh37
NC_000016.8:g.16160914G= NCBI36
NG_007558.2:g.68916C=
NG_007558.3:g.69062C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000622290.5:c.3661C= ENSP00000483331.2:p.Arg1221=
ENST00000205557.12:c.3661C= MANE Select ENSP00000205557.7:p.Arg1221=
ENST00000640696.1:c.475C= ENSP00000492197.1:p.Arg159=
ENST00000205557.11:c.3661C= ENSP00000205557.7:p.Arg1221=
ENST00000456970.6:c.3286C= ENSP00000405002.2:n.3286C=
ENST00000622290.4:c.*870C= ENSP00000483331.1:n.*870C=
NM_001171.5:c.3661C= NP_001162.4:p.Arg1221=
XM_011522479.1:c.3628C= XP_011520781.1:p.Arg1210=
XM_011522480.1:c.3319C= XP_011520782.1:p.Arg1107=
XM_011522481.1:c.3319C= XP_011520783.1:p.Arg1107=
XR_932836.1:n.3896C=
XR_932837.1:n.3697C=
XR_932838.1:n.3697C=
XR_933134.1:n.539-225G=
NM_001351800.1:c.3319C= NP_001338729.1:p.Arg1107=
NR_147784.1:n.3323C=
XM_011522479.2:c.3628C= XP_011520781.1:p.Arg1210=
XM_011522481.3:c.3319C= XP_011520783.1:p.Arg1107=
XM_017023212.1:c.3493C= XP_016878701.1:p.Arg1165=
XM_024450261.1:c.3697C= XP_024306029.1:p.Arg1233=
XR_932836.2:n.3842C=
XR_932837.3:n.3642C=
XR_932838.3:n.3642C=
NM_001171.6:c.3661C= MANE Select NP_001162.5:p.Arg1221=