Canonical Allele Identifier: CA2210140641
Gene: ABCC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.16154779G= , CM000678.2:g.16154779G= GRCh38
NC_000016.9:g.16248636G= , CM000678.1:g.16248636G= GRCh37
NC_000016.8:g.16156137G= NCBI36
NG_007558.2:g.73693C=
NG_007558.3:g.73839C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000576204.6:n.920C=
ENST00000622290.5:c.*229C= ENSP00000483331.2:n.*229C=
ENST00000205557.12:c.4057C= MANE Select ENSP00000205557.7:p.Pro1353=
ENST00000640696.1:c.871C= ENSP00000492197.1:p.Pro291=
ENST00000205557.11:c.4057C= ENSP00000205557.7:p.Pro1353=
ENST00000456970.6:c.3682C= ENSP00000405002.2:n.3682C=
ENST00000576204.5:n.920C=
ENST00000622290.4:c.*1266C= ENSP00000483331.1:n.*1266C=
NM_001171.5:c.4057C= NP_001162.4:p.Pro1353=
XM_011522479.1:c.4024C= XP_011520781.1:p.Pro1342=
XM_011522480.1:c.3715C= XP_011520782.1:p.Pro1239=
XM_011522481.1:c.3715C= XP_011520783.1:p.Pro1239=
XR_933134.1:n.539-5002G=
NM_001351800.1:c.3715C= NP_001338729.1:p.Pro1239=
NR_147784.1:n.3719C=
XM_011522479.2:c.4024C= XP_011520781.1:p.Pro1342=
XM_011522481.3:c.3715C= XP_011520783.1:p.Pro1239=
XM_017023212.1:c.3889C= XP_016878701.1:p.Pro1297=
XM_024450261.1:c.4093C= XP_024306029.1:p.Pro1365=
NM_001171.6:c.4057C= MANE Select NP_001162.5:p.Pro1353=