Canonical Allele Identifier: CA2210131365

Gene: ABCC6

Linked Data

• dbSNP Id: rs2046639378

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16159327_16159328dup , CM000678.2:g.16159327_16159328dup	GRCh38
NC_000016.9:g.16253184_16253185dup , CM000678.1:g.16253184_16253185dup	GRCh37
NC_000016.8:g.16160685_16160686dup	NCBI36
NG_007558.2:g.69145_69146dup
NG_007558.3:g.69291_69292dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.3735+155_3735+156dup	ENSP00000483331.2:n.3735+155_3735+156dup
ENST00000205557.12:c.3735+155_3735+156dup MANE Select	ENSP00000205557.7:n.3735+155_3735+156dup
ENST00000640696.1:c.549+155_549+156dup	ENSP00000492197.1:n.549+155_549+156dup
ENST00000205557.11:c.3735+155_3735+156dup	ENSP00000205557.7:n.3735+155_3735+156dup
ENST00000456970.6:c.3360+155_3360+156dup	ENSP00000405002.2:n.3360+155_3360+156dup
ENST00000622290.4:c.*944+155_*944+156dup	ENSP00000483331.1:n.*944+155_*944+156dup
NM_001171.5:c.3735+155_3735+156dup	NP_001162.4:n.3735+155_3735+156dup
XM_011522479.1:c.3702+155_3702+156dup	XP_011520781.1:n.3702+155_3702+156dup
XM_011522480.1:c.3393+155_3393+156dup	XP_011520782.1:n.3393+155_3393+156dup
XM_011522481.1:c.3393+155_3393+156dup	XP_011520783.1:n.3393+155_3393+156dup
XR_932836.1:n.3970+155_3970+156dup
XR_932837.1:n.3771+155_3771+156dup
XR_932838.1:n.3771+155_3771+156dup
XR_933134.1:n.539-454_539-453dup
NM_001351800.1:c.3393+155_3393+156dup	NP_001338729.1:n.3393+155_3393+156dup
NR_147784.1:n.3397+155_3397+156dup
XM_011522479.2:c.3702+155_3702+156dup	XP_011520781.1:n.3702+155_3702+156dup
XM_011522481.3:c.3393+155_3393+156dup	XP_011520783.1:n.3393+155_3393+156dup
XM_017023212.1:c.3567+155_3567+156dup	XP_016878701.1:n.3567+155_3567+156dup
XM_024450261.1:c.3771+155_3771+156dup	XP_024306029.1:n.3771+155_3771+156dup
XR_932836.2:n.3916+155_3916+156dup
XR_932837.3:n.3716+155_3716+156dup
XR_932838.3:n.3716+155_3716+156dup
NM_001171.6:c.3735+155_3735+156dup MANE Select	NP_001162.5:n.3735+155_3735+156dup