Canonical Allele Identifier: CA2112146368

Gene: ABCC4

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.95186599_95186600delinsAG , CM000675.2:g.95186599_95186600delinsAG	GRCh38
NC_000013.10:g.95838853_95838854delinsAG , CM000675.1:g.95838853_95838854delinsAG	GRCh37
NC_000013.9:g.94636854_94636855delinsAG	NCBI36
NG_050651.1:g.119847_119848delinsCT
NG_050651.2:g.119847_119848delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642524.1:c.*1578+101_*1578+102delinsCT	ENSP00000493766.1:n.*1578+101_*1578+102delinsCT
ENST00000643051.1:c.1545+101_1545+102delinsCT	ENSP00000495513.1:n.1545+101_1545+102delinsCT
ENST00000643556.1:c.1686+101_1686+102delinsCT	ENSP00000494938.1:n.1686+101_1686+102delinsCT
ENST00000643816.1:n.1828+101_1828+102delinsCT
ENST00000643842.1:c.*1591+101_*1591+102delinsCT	ENSP00000493861.1:n.*1591+101_*1591+102delinsCT
ENST00000644471.1:n.1641+101_1641+102delinsCT
ENST00000645237.2:c.1545+101_1545+102delinsCT MANE Select	ENSP00000494609.1:n.1545+101_1545+102delinsCT
ENST00000645532.1:c.1584+101_1584+102delinsCT	ENSP00000494431.1:n.1584+101_1584+102delinsCT
ENST00000646439.1:c.1545+101_1545+102delinsCT	ENSP00000494751.1:n.1545+101_1545+102delinsCT
ENST00000376887.8:c.1545+101_1545+102delinsCT	ENSP00000366084.4:n.1545+101_1545+102delinsCT
ENST00000536256.3:c.1320+101_1320+102delinsCT	ENSP00000442024.1:n.1320+101_1320+102delinsCT
ENST00000629385.1:c.1545+101_1545+102delinsCT	ENSP00000487081.1:n.1545+101_1545+102delinsCT
NM_001105515.2:c.1545+101_1545+102delinsCT	NP_001098985.1:n.1545+101_1545+102delinsCT
NM_001301829.1:c.1545+101_1545+102delinsCT	NP_001288758.1:n.1545+101_1545+102delinsCT
NM_001301830.1:c.1320+101_1320+102delinsCT	NP_001288759.1:n.1320+101_1320+102delinsCT
NM_005845.4:c.1545+101_1545+102delinsCT	NP_005836.2:n.1545+101_1545+102delinsCT
XM_005254025.2:c.1416+101_1416+102delinsCT	XP_005254082.1:n.1416+101_1416+102delinsCT
XM_006719914.1:c.1455+101_1455+102delinsCT	XP_006719977.1:n.1455+101_1455+102delinsCT
XM_011521047.1:c.996+101_996+102delinsCT	XP_011519349.1:n.996+101_996+102delinsCT
XM_017020319.1:c.1416+101_1416+102delinsCT	XP_016875808.1:n.1416+101_1416+102delinsCT
XM_017020320.2:c.1545+101_1545+102delinsCT	XP_016875809.1:n.1545+101_1545+102delinsCT
XM_017020321.1:c.-1091_-1090delinsCT	XP_016875810.1:n.-1091_-1090delinsCT
XM_017020322.1:c.1416+101_1416+102delinsCT	XP_016875811.1:n.1416+101_1416+102delinsCT
NM_001105515.3:c.1545+101_1545+102delinsCT	NP_001098985.1:n.1545+101_1545+102delinsCT
NM_001301829.2:c.1545+101_1545+102delinsCT	NP_001288758.1:n.1545+101_1545+102delinsCT
NM_001301830.2:c.1320+101_1320+102delinsCT	NP_001288759.1:n.1320+101_1320+102delinsCT
NM_005845.5:c.1545+101_1545+102delinsCT MANE Select	NP_005836.2:n.1545+101_1545+102delinsCT