Canonical Allele Identifier: CA2806038104

Gene: ABCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16155209_16155213del , CM000678.2:g.16155209_16155213del	GRCh38
NC_000016.9:g.16249066_16249070del , CM000678.1:g.16249066_16249070del	GRCh37
NC_000016.8:g.16156567_16156571del	NCBI36
NG_007558.2:g.73259_73263del
NG_007558.3:g.73405_73409del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000576204.6:n.564_568del
ENST00000622290.5:c.*55-182_*55-178del	ENSP00000483331.2:n.*55-182_*55-178del
ENST00000205557.12:c.3883-182_3883-178del MANE Select	ENSP00000205557.7:n.3883-182_3883-178del
ENST00000640696.1:c.697-182_697-178del	ENSP00000492197.1:n.697-182_697-178del
ENST00000205557.11:c.3883-182_3883-178del	ENSP00000205557.7:n.3883-182_3883-178del
ENST00000456970.6:c.3508-182_3508-178del	ENSP00000405002.2:n.3508-182_3508-178del
ENST00000576204.5:n.564_568del
ENST00000622290.4:c.*1092-182_*1092-178del	ENSP00000483331.1:n.*1092-182_*1092-178del
NM_001171.5:c.3883-182_3883-178del	NP_001162.4:n.3883-182_3883-178del
XM_011522479.1:c.3850-182_3850-178del	XP_011520781.1:n.3850-182_3850-178del
XM_011522480.1:c.3541-182_3541-178del	XP_011520782.1:n.3541-182_3541-178del
XM_011522481.1:c.3541-182_3541-178del	XP_011520783.1:n.3541-182_3541-178del
XR_932836.1:n.4181-182_4181-178del
XR_932837.1:n.3919-182_3919-178del
XR_932838.1:n.3982-182_3982-178del
XR_933134.1:n.539-4572_539-4568del
NM_001351800.1:c.3541-182_3541-178del	NP_001338729.1:n.3541-182_3541-178del
NR_147784.1:n.3545-182_3545-178del
XM_011522479.2:c.3850-182_3850-178del	XP_011520781.1:n.3850-182_3850-178del
XM_011522481.3:c.3541-182_3541-178del	XP_011520783.1:n.3541-182_3541-178del
XM_017023212.1:c.3715-182_3715-178del	XP_016878701.1:n.3715-182_3715-178del
XM_024450261.1:c.3919-182_3919-178del	XP_024306029.1:n.3919-182_3919-178del
XR_932836.2:n.4127-182_4127-178del
XR_932837.3:n.3864-182_3864-178del
XR_932838.3:n.3927-182_3927-178del
NM_001171.6:c.3883-182_3883-178del MANE Select	NP_001162.5:n.3883-182_3883-178del