Canonical Allele Identifier: CA388403192

Gene: ABCC4

Linked Data

• MyVariant Identifiers: chr13:g.95839127A>G (hg19) ; chr13:g.95186873A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.95186873A>G , CM000675.2:g.95186873A>G	GRCh38
NC_000013.10:g.95839127A>G , CM000675.1:g.95839127A>G	GRCh37
NC_000013.9:g.94637128A>G	NCBI36
NG_050651.1:g.119574T>C
NG_050651.2:g.119574T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642524.1:c.*1406T>C	ENSP00000493766.1:n.*1406T>C
ENST00000643051.1:c.1373T>C	ENSP00000495513.1:p.Val458Ala
ENST00000643556.1:c.1514T>C	ENSP00000494938.1:n.1514T>C
ENST00000643816.1:n.1656T>C
ENST00000643842.1:c.*1419T>C	ENSP00000493861.1:n.*1419T>C
ENST00000644471.1:n.1469T>C
ENST00000645237.2:c.1373T>C MANE Select	ENSP00000494609.1:p.Val458Ala
ENST00000645532.1:c.1412T>C	ENSP00000494431.1:p.Val471Ala
ENST00000646439.1:c.1373T>C	ENSP00000494751.1:p.Val458Ala
ENST00000376887.8:c.1373T>C	ENSP00000366084.4:p.Val458Ala
ENST00000536256.3:c.1148T>C	ENSP00000442024.1:p.Val383Ala
ENST00000629385.1:c.1373T>C	ENSP00000487081.1:p.Val458Ala
NM_001105515.2:c.1373T>C	NP_001098985.1:p.Val458Ala
NM_001301829.1:c.1373T>C	NP_001288758.1:p.Val458Ala
NM_001301830.1:c.1148T>C	NP_001288759.1:p.Val383Ala
NM_005845.4:c.1373T>C	NP_005836.2:p.Val458Ala
XM_005254025.2:c.1244T>C	XP_005254082.1:p.Val415Ala
XM_006719914.1:c.1283T>C	XP_006719977.1:p.Val428Ala
XM_011521047.1:c.824T>C	XP_011519349.1:p.Val275Ala
XM_017020319.1:c.1244T>C	XP_016875808.1:p.Val415Ala
XM_017020320.2:c.1373T>C	XP_016875809.1:p.Val458Ala
XM_017020322.1:c.1244T>C	XP_016875811.1:p.Val415Ala
NM_001105515.3:c.1373T>C	NP_001098985.1:p.Val458Ala
NM_001301829.2:c.1373T>C	NP_001288758.1:p.Val458Ala
NM_001301830.2:c.1148T>C	NP_001288759.1:p.Val383Ala
NM_005845.5:c.1373T>C MANE Select	NP_005836.2:p.Val458Ala