Canonical Allele Identifier: CA394883965

Gene: ABCC6

Linked Data

• MyVariant Identifiers: chr16:g.16244579G>C (hg19) ; chr16:g.16150722G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16150722G>C , CM000678.2:g.16150722G>C	GRCh38
NC_000016.9:g.16244579G>C , CM000678.1:g.16244579G>C	GRCh37
NC_000016.8:g.16152080G>C	NCBI36
NG_007558.2:g.77750C>G
NG_007558.3:g.77896C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.*431C>G	ENSP00000483331.2:n.*431C>G
ENST00000205557.12:c.4259C>G MANE Select	ENSP00000205557.7:p.Thr1420Ser
ENST00000640696.1:c.1073C>G	ENSP00000492197.1:p.Thr358Ser
ENST00000205557.11:c.4259C>G	ENSP00000205557.7:p.Thr1420Ser
ENST00000456970.6:c.3884C>G	ENSP00000405002.2:n.3884C>G
ENST00000576204.5:n.1122C>G
ENST00000622290.4:c.*1468C>G	ENSP00000483331.1:n.*1468C>G
NM_001171.5:c.4259C>G	NP_001162.4:p.Thr1420Ser
XM_011522479.1:c.4226C>G	XP_011520781.1:p.Thr1409Ser
XM_011522480.1:c.3917C>G	XP_011520782.1:p.Thr1306Ser
XM_011522481.1:c.3917C>G	XP_011520783.1:p.Thr1306Ser
XR_933134.1:n.538+6432G>C
NM_001351800.1:c.3917C>G	NP_001338729.1:p.Thr1306Ser
NR_147784.1:n.3921C>G
XM_011522479.2:c.4226C>G	XP_011520781.1:p.Thr1409Ser
XM_011522481.3:c.3917C>G	XP_011520783.1:p.Thr1306Ser
XM_017023212.1:c.4091C>G	XP_016878701.1:p.Thr1364Ser
XM_024450261.1:c.4295C>G	XP_024306029.1:p.Thr1432Ser
NM_001171.6:c.4259C>G MANE Select	NP_001162.5:p.Thr1420Ser