Canonical Allele Identifier: CA493799221

Gene: ABCC6

Linked Data

• MyVariant Identifiers: chr16:g.16244011G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16150154G>C , CM000678.2:g.16150154G>C	GRCh38
NC_000016.9:g.16244011G>C , CM000678.1:g.16244011G>C	GRCh37
NC_000016.8:g.16151512G>C	NCBI36
NG_007558.2:g.78318C>G
NG_007558.3:g.78464C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.*663C>G	ENSP00000483331.2:n.*663C>G
ENST00000205557.12:c.4491C>G MANE Select	ENSP00000205557.7:p.Ala1497=
ENST00000640696.1:c.1305C>G	ENSP00000492197.1:p.Ala435=
ENST00000205557.11:c.4491C>G	ENSP00000205557.7:p.Ala1497=
ENST00000456970.6:c.4116C>G	ENSP00000405002.2:n.4116C>G
ENST00000576204.5:n.1354C>G
ENST00000622290.4:c.*1700C>G	ENSP00000483331.1:n.*1700C>G
NM_001171.5:c.4491C>G	NP_001162.4:p.Ala1497=
XM_011522479.1:c.4458C>G	XP_011520781.1:p.Ala1486=
XM_011522480.1:c.4149C>G	XP_011520782.1:p.Ala1383=
XM_011522481.1:c.4149C>G	XP_011520783.1:p.Ala1383=
XR_933134.1:n.538+5864G>C
NM_001351800.1:c.4149C>G	NP_001338729.1:p.Ala1383=
NR_147784.1:n.4153C>G
XM_011522479.2:c.4458C>G	XP_011520781.1:p.Ala1486=
XM_011522481.3:c.4149C>G	XP_011520783.1:p.Ala1383=
XM_017023212.1:c.4323C>G	XP_016878701.1:p.Ala1441=
XM_024450261.1:c.4527C>G	XP_024306029.1:p.Ala1509=
NM_001171.6:c.4491C>G MANE Select	NP_001162.5:p.Ala1497=