Canonical Allele Identifier: CA2806038107

Gene: ABCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16155213del , CM000678.2:g.16155213del	GRCh38
NC_000016.9:g.16249070del , CM000678.1:g.16249070del	GRCh37
NC_000016.8:g.16156571del	NCBI36
NG_007558.2:g.73260del
NG_007558.3:g.73406del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000576204.6:n.565del
ENST00000622290.5:c.*55-181del	ENSP00000483331.2:n.*55-181del
ENST00000205557.12:c.3883-181del MANE Select	ENSP00000205557.7:n.3883-181del
ENST00000640696.1:c.697-181del	ENSP00000492197.1:n.697-181del
ENST00000205557.11:c.3883-181del	ENSP00000205557.7:n.3883-181del
ENST00000456970.6:c.3508-181del	ENSP00000405002.2:n.3508-181del
ENST00000576204.5:n.565del
ENST00000622290.4:c.*1092-181del	ENSP00000483331.1:n.*1092-181del
NM_001171.5:c.3883-181del	NP_001162.4:n.3883-181del
XM_011522479.1:c.3850-181del	XP_011520781.1:n.3850-181del
XM_011522480.1:c.3541-181del	XP_011520782.1:n.3541-181del
XM_011522481.1:c.3541-181del	XP_011520783.1:n.3541-181del
XR_932836.1:n.4181-181del
XR_932837.1:n.3919-181del
XR_932838.1:n.3982-181del
XR_933134.1:n.539-4568del
NM_001351800.1:c.3541-181del	NP_001338729.1:n.3541-181del
NR_147784.1:n.3545-181del
XM_011522479.2:c.3850-181del	XP_011520781.1:n.3850-181del
XM_011522481.3:c.3541-181del	XP_011520783.1:n.3541-181del
XM_017023212.1:c.3715-181del	XP_016878701.1:n.3715-181del
XM_024450261.1:c.3919-181del	XP_024306029.1:n.3919-181del
XR_932836.2:n.4127-181del
XR_932837.3:n.3864-181del
XR_932838.3:n.3927-181del
NM_001171.6:c.3883-181del MANE Select	NP_001162.5:n.3883-181del