Canonical Allele Identifier: CA2210140925
Gene: ABCC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.16154924A= , CM000678.2:g.16154924A= GRCh38
NC_000016.9:g.16248781A= , CM000678.1:g.16248781A= GRCh37
NC_000016.8:g.16156282A= NCBI36
NG_007558.2:g.73548T=
NG_007558.3:g.73694T=

Transcript Alleles

HGVS Amino-acid change
ENST00000576204.6:n.853T=
ENST00000622290.5:c.*162T= ENSP00000483331.2:n.*162T=
ENST00000205557.12:c.3990T= MANE Select ENSP00000205557.7:p.Ile1330=
ENST00000640696.1:c.804T= ENSP00000492197.1:p.Ile268=
ENST00000205557.11:c.3990T= ENSP00000205557.7:p.Ile1330=
ENST00000456970.6:c.3615T= ENSP00000405002.2:n.3615T=
ENST00000576204.5:n.853T=
ENST00000622290.4:c.*1199T= ENSP00000483331.1:n.*1199T=
NM_001171.5:c.3990T= NP_001162.4:p.Ile1330=
XM_011522479.1:c.3957T= XP_011520781.1:p.Ile1319=
XM_011522480.1:c.3648T= XP_011520782.1:p.Ile1216=
XM_011522481.1:c.3648T= XP_011520783.1:p.Ile1216=
XR_933134.1:n.539-4857A=
NM_001351800.1:c.3648T= NP_001338729.1:p.Ile1216=
NR_147784.1:n.3652T=
XM_011522479.2:c.3957T= XP_011520781.1:p.Ile1319=
XM_011522481.3:c.3648T= XP_011520783.1:p.Ile1216=
XM_017023212.1:c.3822T= XP_016878701.1:p.Ile1274=
XM_024450261.1:c.4026T= XP_024306029.1:p.Ile1342=
NM_001171.6:c.3990T= MANE Select NP_001162.5:p.Ile1330=