Canonical Allele Identifier: CA2806038152
Gene: ABCC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.16155281_16155282insACA , CM000678.2:g.16155281_16155282insACA GRCh38
NC_000016.9:g.16249138_16249139insACA , CM000678.1:g.16249138_16249139insACA GRCh37
NC_000016.8:g.16156639_16156640insACA NCBI36
NG_007558.2:g.73190_73191insTGT
NG_007558.3:g.73336_73337insTGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000576204.6:n.495_496insTGT
ENST00000622290.5:c.*55-251_*55-250insTGT ENSP00000483331.2:n.*55-251_*55-250insTGT
ENST00000205557.12:c.3883-251_3883-250insTGT MANE Select ENSP00000205557.7:n.3883-251_3883-250insTGT
ENST00000640696.1:c.697-251_697-250insTGT ENSP00000492197.1:n.697-251_697-250insTGT
ENST00000205557.11:c.3883-251_3883-250insTGT ENSP00000205557.7:n.3883-251_3883-250insTGT
ENST00000456970.6:c.3508-251_3508-250insTGT ENSP00000405002.2:n.3508-251_3508-250insTGT
ENST00000576204.5:n.495_496insTGT
ENST00000622290.4:c.*1092-251_*1092-250insTGT ENSP00000483331.1:n.*1092-251_*1092-250insTGT
NM_001171.5:c.3883-251_3883-250insTGT NP_001162.4:n.3883-251_3883-250insTGT
XM_011522479.1:c.3850-251_3850-250insTGT XP_011520781.1:n.3850-251_3850-250insTGT
XM_011522480.1:c.3541-251_3541-250insTGT XP_011520782.1:n.3541-251_3541-250insTGT
XM_011522481.1:c.3541-251_3541-250insTGT XP_011520783.1:n.3541-251_3541-250insTGT
XR_932836.1:n.4181-251_4181-250insTGT
XR_932837.1:n.3919-251_3919-250insTGT
XR_932838.1:n.3982-251_3982-250insTGT
XR_933134.1:n.539-4500_539-4499insACA
NM_001351800.1:c.3541-251_3541-250insTGT NP_001338729.1:n.3541-251_3541-250insTGT
NR_147784.1:n.3545-251_3545-250insTGT
XM_011522479.2:c.3850-251_3850-250insTGT XP_011520781.1:n.3850-251_3850-250insTGT
XM_011522481.3:c.3541-251_3541-250insTGT XP_011520783.1:n.3541-251_3541-250insTGT
XM_017023212.1:c.3715-251_3715-250insTGT XP_016878701.1:n.3715-251_3715-250insTGT
XM_024450261.1:c.3919-251_3919-250insTGT XP_024306029.1:n.3919-251_3919-250insTGT
XR_932836.2:n.4127-251_4127-250insTGT
XR_932837.3:n.3864-251_3864-250insTGT
XR_932838.3:n.3927-251_3927-250insTGT
NM_001171.6:c.3883-251_3883-250insTGT MANE Select NP_001162.5:n.3883-251_3883-250insTGT