Canonical Allele Identifier: CA394884097

Gene: ABCC6

Linked Data

• MyVariant Identifiers: chr16:g.16244625C>G (hg19) ; chr16:g.16150768C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16150768C>G , CM000678.2:g.16150768C>G	GRCh38
NC_000016.9:g.16244625C>G , CM000678.1:g.16244625C>G	GRCh37
NC_000016.8:g.16152126C>G	NCBI36
NG_007558.2:g.77704G>C
NG_007558.3:g.77850G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.*385G>C	ENSP00000483331.2:n.*385G>C
ENST00000205557.12:c.4213G>C MANE Select	ENSP00000205557.7:p.Gly1405Arg
ENST00000640696.1:c.1027G>C	ENSP00000492197.1:p.Gly343Arg
ENST00000205557.11:c.4213G>C	ENSP00000205557.7:p.Gly1405Arg
ENST00000456970.6:c.3838G>C	ENSP00000405002.2:n.3838G>C
ENST00000576204.5:n.1076G>C
ENST00000622290.4:c.*1422G>C	ENSP00000483331.1:n.*1422G>C
NM_001171.5:c.4213G>C	NP_001162.4:p.Gly1405Arg
XM_011522479.1:c.4180G>C	XP_011520781.1:p.Gly1394Arg
XM_011522480.1:c.3871G>C	XP_011520782.1:p.Gly1291Arg
XM_011522481.1:c.3871G>C	XP_011520783.1:p.Gly1291Arg
XR_933134.1:n.538+6478C>G
NM_001351800.1:c.3871G>C	NP_001338729.1:p.Gly1291Arg
NR_147784.1:n.3875G>C
XM_011522479.2:c.4180G>C	XP_011520781.1:p.Gly1394Arg
XM_011522481.3:c.3871G>C	XP_011520783.1:p.Gly1291Arg
XM_017023212.1:c.4045G>C	XP_016878701.1:p.Gly1349Arg
XM_024450261.1:c.4249G>C	XP_024306029.1:p.Gly1417Arg
NM_001171.6:c.4213G>C MANE Select	NP_001162.5:p.Gly1405Arg