Canonical Allele Identifier: CA2210139918
Gene: ABCC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.16165724A= , CM000678.2:g.16165724A= GRCh38
NC_000016.9:g.16259581A= , CM000678.1:g.16259581A= GRCh37
NC_000016.8:g.16167082A= NCBI36
NG_007558.2:g.62748T=
NG_007558.3:g.62894T=

Transcript Alleles

HGVS Amino-acid change
ENST00000622290.5:c.3205T= ENSP00000483331.2:p.Tyr1069=
ENST00000205557.12:c.3205T= MANE Select ENSP00000205557.7:p.Tyr1069=
ENST00000640696.1:c.220T= ENSP00000492197.1:p.Tyr74=
ENST00000205557.11:c.3205T= ENSP00000205557.7:p.Tyr1069=
ENST00000456970.6:c.3030T= ENSP00000405002.2:n.3030T=
ENST00000622290.4:c.*414T= ENSP00000483331.1:n.*414T=
NM_001171.5:c.3205T= NP_001162.4:p.Tyr1069=
XM_011522479.1:c.3172T= XP_011520781.1:p.Tyr1058=
XM_011522480.1:c.2863T= XP_011520782.1:p.Tyr955=
XM_011522481.1:c.2863T= XP_011520783.1:p.Tyr955=
XR_932836.1:n.3440T=
XR_932837.1:n.3441T=
XR_932838.1:n.3441T=
NM_001351800.1:c.2863T= NP_001338729.1:p.Tyr955=
NR_147784.1:n.3067T=
XM_011522479.2:c.3172T= XP_011520781.1:p.Tyr1058=
XM_011522481.3:c.2863T= XP_011520783.1:p.Tyr955=
XM_017023212.1:c.3037T= XP_016878701.1:p.Tyr1013=
XM_017023214.1:c.3205T= XP_016878703.1:p.Tyr1069=
XM_024450261.1:c.3241T= XP_024306029.1:p.Tyr1081=
XR_932836.2:n.3386T=
XR_932837.3:n.3386T=
XR_932838.3:n.3386T=
NM_001171.6:c.3205T= MANE Select NP_001162.5:p.Tyr1069=