Canonical Allele Identifier: CA2806038135
Gene: ABCC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.16155236_16155237insACA , CM000678.2:g.16155236_16155237insACA GRCh38
NC_000016.9:g.16249093_16249094insACA , CM000678.1:g.16249093_16249094insACA GRCh37
NC_000016.8:g.16156594_16156595insACA NCBI36
NG_007558.2:g.73235_73236insTGT
NG_007558.3:g.73381_73382insTGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000576204.6:n.540_541insTGT
ENST00000622290.5:c.*55-206_*55-205insTGT ENSP00000483331.2:n.*55-206_*55-205insTGT
ENST00000205557.12:c.3883-206_3883-205insTGT MANE Select ENSP00000205557.7:n.3883-206_3883-205insTGT
ENST00000640696.1:c.697-206_697-205insTGT ENSP00000492197.1:n.697-206_697-205insTGT
ENST00000205557.11:c.3883-206_3883-205insTGT ENSP00000205557.7:n.3883-206_3883-205insTGT
ENST00000456970.6:c.3508-206_3508-205insTGT ENSP00000405002.2:n.3508-206_3508-205insTGT
ENST00000576204.5:n.540_541insTGT
ENST00000622290.4:c.*1092-206_*1092-205insTGT ENSP00000483331.1:n.*1092-206_*1092-205insTGT
NM_001171.5:c.3883-206_3883-205insTGT NP_001162.4:n.3883-206_3883-205insTGT
XM_011522479.1:c.3850-206_3850-205insTGT XP_011520781.1:n.3850-206_3850-205insTGT
XM_011522480.1:c.3541-206_3541-205insTGT XP_011520782.1:n.3541-206_3541-205insTGT
XM_011522481.1:c.3541-206_3541-205insTGT XP_011520783.1:n.3541-206_3541-205insTGT
XR_932836.1:n.4181-206_4181-205insTGT
XR_932837.1:n.3919-206_3919-205insTGT
XR_932838.1:n.3982-206_3982-205insTGT
XR_933134.1:n.539-4545_539-4544insACA
NM_001351800.1:c.3541-206_3541-205insTGT NP_001338729.1:n.3541-206_3541-205insTGT
NR_147784.1:n.3545-206_3545-205insTGT
XM_011522479.2:c.3850-206_3850-205insTGT XP_011520781.1:n.3850-206_3850-205insTGT
XM_011522481.3:c.3541-206_3541-205insTGT XP_011520783.1:n.3541-206_3541-205insTGT
XM_017023212.1:c.3715-206_3715-205insTGT XP_016878701.1:n.3715-206_3715-205insTGT
XM_024450261.1:c.3919-206_3919-205insTGT XP_024306029.1:n.3919-206_3919-205insTGT
XR_932836.2:n.4127-206_4127-205insTGT
XR_932837.3:n.3864-206_3864-205insTGT
XR_932838.3:n.3927-206_3927-205insTGT
NM_001171.6:c.3883-206_3883-205insTGT MANE Select NP_001162.5:n.3883-206_3883-205insTGT