Canonical Allele Identifier: CA394883710

Gene: ABCC6

Linked Data

• MyVariant Identifiers: chr16:g.16244457G>C (hg19) ; chr16:g.16150600G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16150600G>C , CM000678.2:g.16150600G>C	GRCh38
NC_000016.9:g.16244457G>C , CM000678.1:g.16244457G>C	GRCh37
NC_000016.8:g.16151958G>C	NCBI36
NG_007558.2:g.77872C>G
NG_007558.3:g.78018C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.*553C>G	ENSP00000483331.2:n.*553C>G
ENST00000205557.12:c.4381C>G MANE Select	ENSP00000205557.7:p.Arg1461Gly
ENST00000640696.1:c.1195C>G	ENSP00000492197.1:p.Arg399Gly
ENST00000205557.11:c.4381C>G	ENSP00000205557.7:p.Arg1461Gly
ENST00000456970.6:c.4006C>G	ENSP00000405002.2:n.4006C>G
ENST00000576204.5:n.1244C>G
ENST00000622290.4:c.*1590C>G	ENSP00000483331.1:n.*1590C>G
NM_001171.5:c.4381C>G	NP_001162.4:p.Arg1461Gly
XM_011522479.1:c.4348C>G	XP_011520781.1:p.Arg1450Gly
XM_011522480.1:c.4039C>G	XP_011520782.1:p.Arg1347Gly
XM_011522481.1:c.4039C>G	XP_011520783.1:p.Arg1347Gly
XR_933134.1:n.538+6310G>C
NM_001351800.1:c.4039C>G	NP_001338729.1:p.Arg1347Gly
NR_147784.1:n.4043C>G
XM_011522479.2:c.4348C>G	XP_011520781.1:p.Arg1450Gly
XM_011522481.3:c.4039C>G	XP_011520783.1:p.Arg1347Gly
XM_017023212.1:c.4213C>G	XP_016878701.1:p.Arg1405Gly
XM_024450261.1:c.4417C>G	XP_024306029.1:p.Arg1473Gly
NM_001171.6:c.4381C>G MANE Select	NP_001162.5:p.Arg1461Gly