Canonical Allele Identifier: CA2631961384

Gene: ABCC6

Linked Data

• gnomAD v4: 16-16149928-C-CG

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16149931dup , CM000678.2:g.16149931dup	GRCh38
NC_000016.9:g.16243788dup , CM000678.1:g.16243788dup	GRCh37
NC_000016.8:g.16151289dup	NCBI36
NG_007558.2:g.78543dup
NG_007558.3:g.78689dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.*888dup	ENSP00000483331.2:n.*888dup
ENST00000205557.12:c.*204dup MANE Select	ENSP00000205557.7:n.*204dup
ENST00000640696.1:c.1530dup	ENSP00000492197.1:n.1530dup
ENST00000205557.11:c.*204dup	ENSP00000205557.7:n.*204dup
ENST00000576204.5:n.1579dup
ENST00000622290.4:c.*1925dup	ENSP00000483331.1:n.*1925dup
NM_001171.5:c.*204dup	NP_001162.4:n.*204dup
XM_011522479.1:c.*204dup	XP_011520781.1:n.*204dup
XM_011522480.1:c.*204dup	XP_011520782.1:n.*204dup
XM_011522481.1:c.*204dup	XP_011520783.1:n.*204dup
XR_933134.1:n.538+5641dup
NM_001351800.1:c.*204dup	NP_001338729.1:n.*204dup
NR_147784.1:n.4378dup
XM_011522479.2:c.*204dup	XP_011520781.1:n.*204dup
XM_011522481.3:c.*204dup	XP_011520783.1:n.*204dup
XM_017023212.1:c.*204dup	XP_016878701.1:n.*204dup
XM_024450261.1:c.*204dup	XP_024306029.1:n.*204dup
NM_001171.6:c.*204dup MANE Select	NP_001162.5:n.*204dup