Canonical Allele Identifier: CA394884641

Gene: ABCC6

Linked Data

• MyVariant Identifiers: chr16:g.16248586C>G (hg19) ; chr16:g.16154729C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16154729C>G , CM000678.2:g.16154729C>G	GRCh38
NC_000016.9:g.16248586C>G , CM000678.1:g.16248586C>G	GRCh37
NC_000016.8:g.16156087C>G	NCBI36
NG_007558.2:g.73743G>C
NG_007558.3:g.73889G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.*279G>C	ENSP00000483331.2:n.*279G>C
ENST00000205557.12:c.4107G>C MANE Select	ENSP00000205557.7:p.Glu1369Asp
ENST00000640696.1:c.921G>C	ENSP00000492197.1:p.Glu307Asp
ENST00000205557.11:c.4107G>C	ENSP00000205557.7:p.Glu1369Asp
ENST00000456970.6:c.3732G>C	ENSP00000405002.2:n.3732G>C
ENST00000576204.5:n.970G>C
ENST00000622290.4:c.*1316G>C	ENSP00000483331.1:n.*1316G>C
NM_001171.5:c.4107G>C	NP_001162.4:p.Glu1369Asp
XM_011522479.1:c.4074G>C	XP_011520781.1:p.Glu1358Asp
XM_011522480.1:c.3765G>C	XP_011520782.1:p.Glu1255Asp
XM_011522481.1:c.3765G>C	XP_011520783.1:p.Glu1255Asp
XR_933134.1:n.539-5052C>G
NM_001351800.1:c.3765G>C	NP_001338729.1:p.Glu1255Asp
NR_147784.1:n.3769G>C
XM_011522479.2:c.4074G>C	XP_011520781.1:p.Glu1358Asp
XM_011522481.3:c.3765G>C	XP_011520783.1:p.Glu1255Asp
XM_017023212.1:c.3939G>C	XP_016878701.1:p.Glu1313Asp
XM_024450261.1:c.4143G>C	XP_024306029.1:p.Glu1381Asp
NM_001171.6:c.4107G>C MANE Select	NP_001162.5:p.Glu1369Asp