Canonical Allele Identifier: CA2210136973
Gene: ABCC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.16163172T= , CM000678.2:g.16163172T= GRCh38
NC_000016.9:g.16257029T= , CM000678.1:g.16257029T= GRCh37
NC_000016.8:g.16164530T= NCBI36
NG_007558.2:g.65300A=
NG_007558.3:g.65446A=

Transcript Alleles

HGVS Amino-acid change
ENST00000622290.5:c.3327A= ENSP00000483331.2:p.Ser1109=
ENST00000205557.12:c.3327A= MANE Select ENSP00000205557.7:p.Ser1109=
ENST00000640696.1:c.321-1608A= ENSP00000492197.1:n.321-1608A=
ENST00000205557.11:c.3327A= ENSP00000205557.7:p.Ser1109=
ENST00000456970.6:c.3132-1608A= ENSP00000405002.2:n.3132-1608A=
ENST00000622290.4:c.*536A= ENSP00000483331.1:n.*536A=
NM_001171.5:c.3327A= NP_001162.4:p.Ser1109=
XM_011522479.1:c.3294A= XP_011520781.1:p.Ser1098=
XM_011522480.1:c.2985A= XP_011520782.1:p.Ser995=
XM_011522481.1:c.2985A= XP_011520783.1:p.Ser995=
XR_932836.1:n.3562A=
XR_932837.1:n.3543-1608A=
XR_932838.1:n.3543-1608A=
XR_933133.1:n.407+329T=
XR_933134.1:n.754+329T=
NM_001351800.1:c.2985A= NP_001338729.1:p.Ser995=
NR_147784.1:n.3169-1608A=
XM_011522479.2:c.3294A= XP_011520781.1:p.Ser1098=
XM_011522481.3:c.2985A= XP_011520783.1:p.Ser995=
XM_017023212.1:c.3159A= XP_016878701.1:p.Ser1053=
XM_017023214.1:c.3307-1608A= XP_016878703.1:n.3307-1608A=
XM_024450261.1:c.3363A= XP_024306029.1:p.Ser1121=
XR_932836.2:n.3508A=
XR_932837.3:n.3488-1608A=
XR_932838.3:n.3488-1608A=
NM_001171.6:c.3327A= MANE Select NP_001162.5:p.Ser1109=