Canonical Allele Identifier: CA493799278

Gene: ABCC6

Linked Data

• MyVariant Identifiers: chr16:g.16244071C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16150214C>A , CM000678.2:g.16150214C>A	GRCh38
NC_000016.9:g.16244071C>A , CM000678.1:g.16244071C>A	GRCh37
NC_000016.8:g.16151572C>A	NCBI36
NG_007558.2:g.78258G>T
NG_007558.3:g.78404G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.*603G>T	ENSP00000483331.2:n.*603G>T
ENST00000205557.12:c.4431G>T MANE Select	ENSP00000205557.7:p.Val1477=
ENST00000640696.1:c.1245G>T	ENSP00000492197.1:p.Val415=
ENST00000205557.11:c.4431G>T	ENSP00000205557.7:p.Val1477=
ENST00000456970.6:c.4056G>T	ENSP00000405002.2:n.4056G>T
ENST00000576204.5:n.1294G>T
ENST00000622290.4:c.*1640G>T	ENSP00000483331.1:n.*1640G>T
NM_001171.5:c.4431G>T	NP_001162.4:p.Val1477=
XM_011522479.1:c.4398G>T	XP_011520781.1:p.Val1466=
XM_011522480.1:c.4089G>T	XP_011520782.1:p.Val1363=
XM_011522481.1:c.4089G>T	XP_011520783.1:p.Val1363=
XR_933134.1:n.538+5924C>A
NM_001351800.1:c.4089G>T	NP_001338729.1:p.Val1363=
NR_147784.1:n.4093G>T
XM_011522479.2:c.4398G>T	XP_011520781.1:p.Val1466=
XM_011522481.3:c.4089G>T	XP_011520783.1:p.Val1363=
XM_017023212.1:c.4263G>T	XP_016878701.1:p.Val1421=
XM_024450261.1:c.4467G>T	XP_024306029.1:p.Val1489=
NM_001171.6:c.4431G>T MANE Select	NP_001162.5:p.Val1477=