Canonical Allele Identifier: CA2806038100
Gene: ABCC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.16155206_16155207insACA , CM000678.2:g.16155206_16155207insACA GRCh38
NC_000016.9:g.16249063_16249064insACA , CM000678.1:g.16249063_16249064insACA GRCh37
NC_000016.8:g.16156564_16156565insACA NCBI36
NG_007558.2:g.73265_73266insTGT
NG_007558.3:g.73411_73412insTGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000576204.6:n.570_571insTGT
ENST00000622290.5:c.*55-176_*55-175insTGT ENSP00000483331.2:n.*55-176_*55-175insTGT
ENST00000205557.12:c.3883-176_3883-175insTGT MANE Select ENSP00000205557.7:n.3883-176_3883-175insTGT
ENST00000640696.1:c.697-176_697-175insTGT ENSP00000492197.1:n.697-176_697-175insTGT
ENST00000205557.11:c.3883-176_3883-175insTGT ENSP00000205557.7:n.3883-176_3883-175insTGT
ENST00000456970.6:c.3508-176_3508-175insTGT ENSP00000405002.2:n.3508-176_3508-175insTGT
ENST00000576204.5:n.570_571insTGT
ENST00000622290.4:c.*1092-176_*1092-175insTGT ENSP00000483331.1:n.*1092-176_*1092-175insTGT
NM_001171.5:c.3883-176_3883-175insTGT NP_001162.4:n.3883-176_3883-175insTGT
XM_011522479.1:c.3850-176_3850-175insTGT XP_011520781.1:n.3850-176_3850-175insTGT
XM_011522480.1:c.3541-176_3541-175insTGT XP_011520782.1:n.3541-176_3541-175insTGT
XM_011522481.1:c.3541-176_3541-175insTGT XP_011520783.1:n.3541-176_3541-175insTGT
XR_932836.1:n.4181-176_4181-175insTGT
XR_932837.1:n.3919-176_3919-175insTGT
XR_932838.1:n.3982-176_3982-175insTGT
XR_933134.1:n.539-4575_539-4574insACA
NM_001351800.1:c.3541-176_3541-175insTGT NP_001338729.1:n.3541-176_3541-175insTGT
NR_147784.1:n.3545-176_3545-175insTGT
XM_011522479.2:c.3850-176_3850-175insTGT XP_011520781.1:n.3850-176_3850-175insTGT
XM_011522481.3:c.3541-176_3541-175insTGT XP_011520783.1:n.3541-176_3541-175insTGT
XM_017023212.1:c.3715-176_3715-175insTGT XP_016878701.1:n.3715-176_3715-175insTGT
XM_024450261.1:c.3919-176_3919-175insTGT XP_024306029.1:n.3919-176_3919-175insTGT
XR_932836.2:n.4127-176_4127-175insTGT
XR_932837.3:n.3864-176_3864-175insTGT
XR_932838.3:n.3927-176_3927-175insTGT
NM_001171.6:c.3883-176_3883-175insTGT MANE Select NP_001162.5:n.3883-176_3883-175insTGT