Canonical Allele Identifier: CA484498176

Gene: ABCC4

Linked Data

• MyVariant Identifiers: chr13:g.95839108T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.95186854T>G , CM000675.2:g.95186854T>G	GRCh38
NC_000013.10:g.95839108T>G , CM000675.1:g.95839108T>G	GRCh37
NC_000013.9:g.94637109T>G	NCBI36
NG_050651.1:g.119593A>C
NG_050651.2:g.119593A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642524.1:c.*1425A>C	ENSP00000493766.1:n.*1425A>C
ENST00000643051.1:c.1392A>C	ENSP00000495513.1:p.Pro464=
ENST00000643556.1:c.1533A>C	ENSP00000494938.1:n.1533A>C
ENST00000643816.1:n.1675A>C
ENST00000643842.1:c.*1438A>C	ENSP00000493861.1:n.*1438A>C
ENST00000644471.1:n.1488A>C
ENST00000645237.2:c.1392A>C MANE Select	ENSP00000494609.1:p.Pro464=
ENST00000645532.1:c.1431A>C	ENSP00000494431.1:p.Pro477=
ENST00000646439.1:c.1392A>C	ENSP00000494751.1:p.Pro464=
ENST00000376887.8:c.1392A>C	ENSP00000366084.4:p.Pro464=
ENST00000536256.3:c.1167A>C	ENSP00000442024.1:p.Pro389=
ENST00000629385.1:c.1392A>C	ENSP00000487081.1:p.Pro464=
NM_001105515.2:c.1392A>C	NP_001098985.1:p.Pro464=
NM_001301829.1:c.1392A>C	NP_001288758.1:p.Pro464=
NM_001301830.1:c.1167A>C	NP_001288759.1:p.Pro389=
NM_005845.4:c.1392A>C	NP_005836.2:p.Pro464=
XM_005254025.2:c.1263A>C	XP_005254082.1:p.Pro421=
XM_006719914.1:c.1302A>C	XP_006719977.1:p.Pro434=
XM_011521047.1:c.843A>C	XP_011519349.1:p.Pro281=
XM_017020319.1:c.1263A>C	XP_016875808.1:p.Pro421=
XM_017020320.2:c.1392A>C	XP_016875809.1:p.Pro464=
XM_017020322.1:c.1263A>C	XP_016875811.1:p.Pro421=
NM_001105515.3:c.1392A>C	NP_001098985.1:p.Pro464=
NM_001301829.2:c.1392A>C	NP_001288758.1:p.Pro464=
NM_001301830.2:c.1167A>C	NP_001288759.1:p.Pro389=
NM_005845.5:c.1392A>C MANE Select	NP_005836.2:p.Pro464=