Canonical Allele Identifier: CA2210141310
Gene: ABCC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.16155249A= , CM000678.2:g.16155249A= GRCh38
NC_000016.9:g.16249106A= , CM000678.1:g.16249106A= GRCh37
NC_000016.8:g.16156607A= NCBI36
NG_007558.2:g.73223T=
NG_007558.3:g.73369T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000576204.6:n.528T=
ENST00000622290.5:c.*55-218T= ENSP00000483331.2:n.*55-218T=
ENST00000205557.12:c.3883-218T= MANE Select ENSP00000205557.7:n.3883-218T=
ENST00000640696.1:c.697-218T= ENSP00000492197.1:n.697-218T=
ENST00000205557.11:c.3883-218T= ENSP00000205557.7:n.3883-218T=
ENST00000456970.6:c.3508-218T= ENSP00000405002.2:n.3508-218T=
ENST00000576204.5:n.528T=
ENST00000622290.4:c.*1092-218T= ENSP00000483331.1:n.*1092-218T=
NM_001171.5:c.3883-218T= NP_001162.4:n.3883-218T=
XM_011522479.1:c.3850-218T= XP_011520781.1:n.3850-218T=
XM_011522480.1:c.3541-218T= XP_011520782.1:n.3541-218T=
XM_011522481.1:c.3541-218T= XP_011520783.1:n.3541-218T=
XR_932836.1:n.4181-218T=
XR_932837.1:n.3919-218T=
XR_932838.1:n.3982-218T=
XR_933134.1:n.539-4532A=
NM_001351800.1:c.3541-218T= NP_001338729.1:n.3541-218T=
NR_147784.1:n.3545-218T=
XM_011522479.2:c.3850-218T= XP_011520781.1:n.3850-218T=
XM_011522481.3:c.3541-218T= XP_011520783.1:n.3541-218T=
XM_017023212.1:c.3715-218T= XP_016878701.1:n.3715-218T=
XM_024450261.1:c.3919-218T= XP_024306029.1:n.3919-218T=
XR_932836.2:n.4127-218T=
XR_932837.3:n.3864-218T=
XR_932838.3:n.3927-218T=
NM_001171.6:c.3883-218T= MANE Select NP_001162.5:n.3883-218T=