Canonical Allele Identifier: CA2210131836
Gene: ABCC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.16159509C= , CM000678.2:g.16159509C= GRCh38
NC_000016.9:g.16253366C= , CM000678.1:g.16253366C= GRCh37
NC_000016.8:g.16160867C= NCBI36
NG_007558.2:g.68963G=
NG_007558.3:g.69109G=

Transcript Alleles

HGVS Amino-acid change
ENST00000622290.5:c.3708G= ENSP00000483331.2:p.Met1236=
ENST00000205557.12:c.3708G= MANE Select ENSP00000205557.7:p.Met1236=
ENST00000640696.1:c.522G= ENSP00000492197.1:p.Met174=
ENST00000205557.11:c.3708G= ENSP00000205557.7:p.Met1236=
ENST00000456970.6:c.3333G= ENSP00000405002.2:n.3333G=
ENST00000622290.4:c.*917G= ENSP00000483331.1:n.*917G=
NM_001171.5:c.3708G= NP_001162.4:p.Met1236=
XM_011522479.1:c.3675G= XP_011520781.1:p.Met1225=
XM_011522480.1:c.3366G= XP_011520782.1:p.Met1122=
XM_011522481.1:c.3366G= XP_011520783.1:p.Met1122=
XR_932836.1:n.3943G=
XR_932837.1:n.3744G=
XR_932838.1:n.3744G=
XR_933134.1:n.539-272C=
NM_001351800.1:c.3366G= NP_001338729.1:p.Met1122=
NR_147784.1:n.3370G=
XM_011522479.2:c.3675G= XP_011520781.1:p.Met1225=
XM_011522481.3:c.3366G= XP_011520783.1:p.Met1122=
XM_017023212.1:c.3540G= XP_016878701.1:p.Met1180=
XM_024450261.1:c.3744G= XP_024306029.1:p.Met1248=
XR_932836.2:n.3889G=
XR_932837.3:n.3689G=
XR_932838.3:n.3689G=
NM_001171.6:c.3708G= MANE Select NP_001162.5:p.Met1236=