Canonical Allele Identifier: CA2806038060
Gene: ABCC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.16155179_16155180insAG , CM000678.2:g.16155179_16155180insAG GRCh38
NC_000016.9:g.16249036_16249037insAG , CM000678.1:g.16249036_16249037insAG GRCh37
NC_000016.8:g.16156537_16156538insAG NCBI36
NG_007558.2:g.73292_73293insCT
NG_007558.3:g.73438_73439insCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000576204.6:n.597_598insCT
ENST00000622290.5:c.*55-149_*55-148insCT ENSP00000483331.2:n.*55-149_*55-148insCT
ENST00000205557.12:c.3883-149_3883-148insCT MANE Select ENSP00000205557.7:n.3883-149_3883-148insCT
ENST00000640696.1:c.697-149_697-148insCT ENSP00000492197.1:n.697-149_697-148insCT
ENST00000205557.11:c.3883-149_3883-148insCT ENSP00000205557.7:n.3883-149_3883-148insCT
ENST00000456970.6:c.3508-149_3508-148insCT ENSP00000405002.2:n.3508-149_3508-148insCT
ENST00000576204.5:n.597_598insCT
ENST00000622290.4:c.*1092-149_*1092-148insCT ENSP00000483331.1:n.*1092-149_*1092-148insCT
NM_001171.5:c.3883-149_3883-148insCT NP_001162.4:n.3883-149_3883-148insCT
XM_011522479.1:c.3850-149_3850-148insCT XP_011520781.1:n.3850-149_3850-148insCT
XM_011522480.1:c.3541-149_3541-148insCT XP_011520782.1:n.3541-149_3541-148insCT
XM_011522481.1:c.3541-149_3541-148insCT XP_011520783.1:n.3541-149_3541-148insCT
XR_932836.1:n.4181-149_4181-148insCT
XR_932837.1:n.3919-149_3919-148insCT
XR_932838.1:n.3982-149_3982-148insCT
XR_933134.1:n.539-4602_539-4601insAG
NM_001351800.1:c.3541-149_3541-148insCT NP_001338729.1:n.3541-149_3541-148insCT
NR_147784.1:n.3545-149_3545-148insCT
XM_011522479.2:c.3850-149_3850-148insCT XP_011520781.1:n.3850-149_3850-148insCT
XM_011522481.3:c.3541-149_3541-148insCT XP_011520783.1:n.3541-149_3541-148insCT
XM_017023212.1:c.3715-149_3715-148insCT XP_016878701.1:n.3715-149_3715-148insCT
XM_024450261.1:c.3919-149_3919-148insCT XP_024306029.1:n.3919-149_3919-148insCT
XR_932836.2:n.4127-149_4127-148insCT
XR_932837.3:n.3864-149_3864-148insCT
XR_932838.3:n.3927-149_3927-148insCT
NM_001171.6:c.3883-149_3883-148insCT MANE Select NP_001162.5:n.3883-149_3883-148insCT