Canonical Allele Identifier: CA2210131994
Gene: ABCC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.16159552T= , CM000678.2:g.16159552T= GRCh38
NC_000016.9:g.16253409T= , CM000678.1:g.16253409T= GRCh37
NC_000016.8:g.16160910T= NCBI36
NG_007558.2:g.68920A=
NG_007558.3:g.69066A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000622290.5:c.3665A= ENSP00000483331.2:p.Asn1222=
ENST00000205557.12:c.3665A= MANE Select ENSP00000205557.7:p.Asn1222=
ENST00000640696.1:c.479A= ENSP00000492197.1:p.Asn160=
ENST00000205557.11:c.3665A= ENSP00000205557.7:p.Asn1222=
ENST00000456970.6:c.3290A= ENSP00000405002.2:n.3290A=
ENST00000622290.4:c.*874A= ENSP00000483331.1:n.*874A=
NM_001171.5:c.3665A= NP_001162.4:p.Asn1222=
XM_011522479.1:c.3632A= XP_011520781.1:p.Asn1211=
XM_011522480.1:c.3323A= XP_011520782.1:p.Asn1108=
XM_011522481.1:c.3323A= XP_011520783.1:p.Asn1108=
XR_932836.1:n.3900A=
XR_932837.1:n.3701A=
XR_932838.1:n.3701A=
XR_933134.1:n.539-229T=
NM_001351800.1:c.3323A= NP_001338729.1:p.Asn1108=
NR_147784.1:n.3327A=
XM_011522479.2:c.3632A= XP_011520781.1:p.Asn1211=
XM_011522481.3:c.3323A= XP_011520783.1:p.Asn1108=
XM_017023212.1:c.3497A= XP_016878701.1:p.Asn1166=
XM_024450261.1:c.3701A= XP_024306029.1:p.Asn1234=
XR_932836.2:n.3846A=
XR_932837.3:n.3646A=
XR_932838.3:n.3646A=
NM_001171.6:c.3665A= MANE Select NP_001162.5:p.Asn1222=