Canonical Allele Identifier: CA394883810

Gene: ABCC6

Linked Data

• MyVariant Identifiers: chr16:g.16244504C>T (hg19) ; chr16:g.16150647C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16150647C>T , CM000678.2:g.16150647C>T	GRCh38
NC_000016.9:g.16244504C>T , CM000678.1:g.16244504C>T	GRCh37
NC_000016.8:g.16152005C>T	NCBI36
NG_007558.2:g.77825G>A
NG_007558.3:g.77971G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.*506G>A	ENSP00000483331.2:n.*506G>A
ENST00000205557.12:c.4334G>A MANE Select	ENSP00000205557.7:p.Gly1445Glu
ENST00000640696.1:c.1148G>A	ENSP00000492197.1:p.Gly383Glu
ENST00000205557.11:c.4334G>A	ENSP00000205557.7:p.Gly1445Glu
ENST00000456970.6:c.3959G>A	ENSP00000405002.2:n.3959G>A
ENST00000576204.5:n.1197G>A
ENST00000622290.4:c.*1543G>A	ENSP00000483331.1:n.*1543G>A
NM_001171.5:c.4334G>A	NP_001162.4:p.Gly1445Glu
XM_011522479.1:c.4301G>A	XP_011520781.1:p.Gly1434Glu
XM_011522480.1:c.3992G>A	XP_011520782.1:p.Gly1331Glu
XM_011522481.1:c.3992G>A	XP_011520783.1:p.Gly1331Glu
XR_933134.1:n.538+6357C>T
NM_001351800.1:c.3992G>A	NP_001338729.1:p.Gly1331Glu
NR_147784.1:n.3996G>A
XM_011522479.2:c.4301G>A	XP_011520781.1:p.Gly1434Glu
XM_011522481.3:c.3992G>A	XP_011520783.1:p.Gly1331Glu
XM_017023212.1:c.4166G>A	XP_016878701.1:p.Gly1389Glu
XM_024450261.1:c.4370G>A	XP_024306029.1:p.Gly1457Glu
NM_001171.6:c.4334G>A MANE Select	NP_001162.5:p.Gly1445Glu