Canonical Allele Identifier: CA484498185

Gene: ABCC4

Linked Data

• dbSNP Id: rs2038081883
• MyVariant Identifiers: chr13:g.95839120C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.95186866C>T , CM000675.2:g.95186866C>T	GRCh38
NC_000013.10:g.95839120C>T , CM000675.1:g.95839120C>T	GRCh37
NC_000013.9:g.94637121C>T	NCBI36
NG_050651.1:g.119581G>A
NG_050651.2:g.119581G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642524.1:c.*1413G>A	ENSP00000493766.1:n.*1413G>A
ENST00000643051.1:c.1380G>A	ENSP00000495513.1:p.Gly460=
ENST00000643556.1:c.1521G>A	ENSP00000494938.1:n.1521G>A
ENST00000643816.1:n.1663G>A
ENST00000643842.1:c.*1426G>A	ENSP00000493861.1:n.*1426G>A
ENST00000644471.1:n.1476G>A
ENST00000645237.2:c.1380G>A MANE Select	ENSP00000494609.1:p.Gly460=
ENST00000645532.1:c.1419G>A	ENSP00000494431.1:p.Gly473=
ENST00000646439.1:c.1380G>A	ENSP00000494751.1:p.Gly460=
ENST00000376887.8:c.1380G>A	ENSP00000366084.4:p.Gly460=
ENST00000536256.3:c.1155G>A	ENSP00000442024.1:p.Gly385=
ENST00000629385.1:c.1380G>A	ENSP00000487081.1:p.Gly460=
NM_001105515.2:c.1380G>A	NP_001098985.1:p.Gly460=
NM_001301829.1:c.1380G>A	NP_001288758.1:p.Gly460=
NM_001301830.1:c.1155G>A	NP_001288759.1:p.Gly385=
NM_005845.4:c.1380G>A	NP_005836.2:p.Gly460=
XM_005254025.2:c.1251G>A	XP_005254082.1:p.Gly417=
XM_006719914.1:c.1290G>A	XP_006719977.1:p.Gly430=
XM_011521047.1:c.831G>A	XP_011519349.1:p.Gly277=
XM_017020319.1:c.1251G>A	XP_016875808.1:p.Gly417=
XM_017020320.2:c.1380G>A	XP_016875809.1:p.Gly460=
XM_017020322.1:c.1251G>A	XP_016875811.1:p.Gly417=
NM_001105515.3:c.1380G>A	NP_001098985.1:p.Gly460=
NM_001301829.2:c.1380G>A	NP_001288758.1:p.Gly460=
NM_001301830.2:c.1155G>A	NP_001288759.1:p.Gly385=
NM_005845.5:c.1380G>A MANE Select	NP_005836.2:p.Gly460=