Canonical Allele Identifier: CA2806038037

Gene: ABCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16155172del , CM000678.2:g.16155172del	GRCh38
NC_000016.9:g.16249029del , CM000678.1:g.16249029del	GRCh37
NC_000016.8:g.16156530del	NCBI36
NG_007558.2:g.73300del
NG_007558.3:g.73446del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000576204.6:n.605del
ENST00000622290.5:c.*55-141del	ENSP00000483331.2:n.*55-141del
ENST00000205557.12:c.3883-141del MANE Select	ENSP00000205557.7:n.3883-141del
ENST00000640696.1:c.697-141del	ENSP00000492197.1:n.697-141del
ENST00000205557.11:c.3883-141del	ENSP00000205557.7:n.3883-141del
ENST00000456970.6:c.3508-141del	ENSP00000405002.2:n.3508-141del
ENST00000576204.5:n.605del
ENST00000622290.4:c.*1092-141del	ENSP00000483331.1:n.*1092-141del
NM_001171.5:c.3883-141del	NP_001162.4:n.3883-141del
XM_011522479.1:c.3850-141del	XP_011520781.1:n.3850-141del
XM_011522480.1:c.3541-141del	XP_011520782.1:n.3541-141del
XM_011522481.1:c.3541-141del	XP_011520783.1:n.3541-141del
XR_932836.1:n.4181-141del
XR_932837.1:n.3919-141del
XR_932838.1:n.3982-141del
XR_933134.1:n.539-4609del
NM_001351800.1:c.3541-141del	NP_001338729.1:n.3541-141del
NR_147784.1:n.3545-141del
XM_011522479.2:c.3850-141del	XP_011520781.1:n.3850-141del
XM_011522481.3:c.3541-141del	XP_011520783.1:n.3541-141del
XM_017023212.1:c.3715-141del	XP_016878701.1:n.3715-141del
XM_024450261.1:c.3919-141del	XP_024306029.1:n.3919-141del
XR_932836.2:n.4127-141del
XR_932837.3:n.3864-141del
XR_932838.3:n.3927-141del
NM_001171.6:c.3883-141del MANE Select	NP_001162.5:n.3883-141del