Canonical Allele Identifier: CA484498108

Gene: ABCC4

Linked Data

• MyVariant Identifiers: chr13:g.95839054G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.95186800G>T , CM000675.2:g.95186800G>T	GRCh38
NC_000013.10:g.95839054G>T , CM000675.1:g.95839054G>T	GRCh37
NC_000013.9:g.94637055G>T	NCBI36
NG_050651.1:g.119647C>A
NG_050651.2:g.119647C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642524.1:c.*1479C>A	ENSP00000493766.1:n.*1479C>A
ENST00000643051.1:c.1446C>A	ENSP00000495513.1:p.Pro482=
ENST00000643556.1:c.1587C>A	ENSP00000494938.1:n.1587C>A
ENST00000643816.1:n.1729C>A
ENST00000643842.1:c.*1492C>A	ENSP00000493861.1:n.*1492C>A
ENST00000644471.1:n.1542C>A
ENST00000645237.2:c.1446C>A MANE Select	ENSP00000494609.1:p.Pro482=
ENST00000645532.1:c.1485C>A	ENSP00000494431.1:p.Pro495=
ENST00000646439.1:c.1446C>A	ENSP00000494751.1:p.Pro482=
ENST00000376887.8:c.1446C>A	ENSP00000366084.4:p.Pro482=
ENST00000536256.3:c.1221C>A	ENSP00000442024.1:p.Pro407=
ENST00000629385.1:c.1446C>A	ENSP00000487081.1:p.Pro482=
NM_001105515.2:c.1446C>A	NP_001098985.1:p.Pro482=
NM_001301829.1:c.1446C>A	NP_001288758.1:p.Pro482=
NM_001301830.1:c.1221C>A	NP_001288759.1:p.Pro407=
NM_005845.4:c.1446C>A	NP_005836.2:p.Pro482=
XM_005254025.2:c.1317C>A	XP_005254082.1:p.Pro439=
XM_006719914.1:c.1356C>A	XP_006719977.1:p.Pro452=
XM_011521047.1:c.897C>A	XP_011519349.1:p.Pro299=
XM_017020319.1:c.1317C>A	XP_016875808.1:p.Pro439=
XM_017020320.2:c.1446C>A	XP_016875809.1:p.Pro482=
XM_017020322.1:c.1317C>A	XP_016875811.1:p.Pro439=
NM_001105515.3:c.1446C>A	NP_001098985.1:p.Pro482=
NM_001301829.2:c.1446C>A	NP_001288758.1:p.Pro482=
NM_001301830.2:c.1221C>A	NP_001288759.1:p.Pro407=
NM_005845.5:c.1446C>A MANE Select	NP_005836.2:p.Pro482=