Canonical Allele Identifier: CA394875641

Gene: ABCC6

Linked Data

• MyVariant Identifiers: chr16:g.16248793G>C (hg19) ; chr16:g.16154936G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16154936G>C , CM000678.2:g.16154936G>C	GRCh38
NC_000016.9:g.16248793G>C , CM000678.1:g.16248793G>C	GRCh37
NC_000016.8:g.16156294G>C	NCBI36
NG_007558.2:g.73536C>G
NG_007558.3:g.73682C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000576204.6:n.841C>G
ENST00000622290.5:c.*150C>G	ENSP00000483331.2:n.*150C>G
ENST00000205557.12:c.3978C>G MANE Select	ENSP00000205557.7:p.Asp1326Glu
ENST00000640696.1:c.792C>G	ENSP00000492197.1:p.Asp264Glu
ENST00000205557.11:c.3978C>G	ENSP00000205557.7:p.Asp1326Glu
ENST00000456970.6:c.3603C>G	ENSP00000405002.2:n.3603C>G
ENST00000576204.5:n.841C>G
ENST00000622290.4:c.*1187C>G	ENSP00000483331.1:n.*1187C>G
NM_001171.5:c.3978C>G	NP_001162.4:p.Asp1326Glu
XM_011522479.1:c.3945C>G	XP_011520781.1:p.Asp1315Glu
XM_011522480.1:c.3636C>G	XP_011520782.1:p.Asp1212Glu
XM_011522481.1:c.3636C>G	XP_011520783.1:p.Asp1212Glu
XR_933134.1:n.539-4845G>C
NM_001351800.1:c.3636C>G	NP_001338729.1:p.Asp1212Glu
NR_147784.1:n.3640C>G
XM_011522479.2:c.3945C>G	XP_011520781.1:p.Asp1315Glu
XM_011522481.3:c.3636C>G	XP_011520783.1:p.Asp1212Glu
XM_017023212.1:c.3810C>G	XP_016878701.1:p.Asp1270Glu
XM_024450261.1:c.4014C>G	XP_024306029.1:p.Asp1338Glu
NM_001171.6:c.3978C>G MANE Select	NP_001162.5:p.Asp1326Glu