Canonical Allele Identifier: CA484496525

Gene: ABCC4

Linked Data

• dbSNP Id: rs1346486475
• gnomAD v2: 13-95822804-C-T
• gnomAD v4: 13-95170550-C-T
• MyVariant Identifiers: chr13:g.95822804C>T (hg19) ; chr13:g.95170550C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.95170550C>T , CM000675.2:g.95170550C>T	GRCh38
NC_000013.10:g.95822804C>T , CM000675.1:g.95822804C>T	GRCh37
NC_000013.9:g.94620805C>T	NCBI36
NG_050651.1:g.135897G>A
NG_050651.2:g.135897G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642524.1:c.*1839G>A	ENSP00000493766.1:n.*1839G>A
ENST00000643051.1:c.1806G>A	ENSP00000495513.1:p.Gln602=
ENST00000643556.1:c.1947G>A	ENSP00000494938.1:n.1947G>A
ENST00000643816.1:n.2089G>A
ENST00000643842.1:c.*1852G>A	ENSP00000493861.1:n.*1852G>A
ENST00000644471.1:n.1897G>A
ENST00000645237.2:c.1806G>A MANE Select	ENSP00000494609.1:p.Gln602=
ENST00000645532.1:c.1845G>A	ENSP00000494431.1:p.Gln615=
ENST00000646439.1:c.1806G>A	ENSP00000494751.1:p.Gln602=
ENST00000376887.8:c.1806G>A	ENSP00000366084.4:p.Gln602=
ENST00000536256.3:c.1581G>A	ENSP00000442024.1:p.Gln527=
ENST00000629385.1:c.1806G>A	ENSP00000487081.1:p.Gln602=
NM_001105515.2:c.1806G>A	NP_001098985.1:p.Gln602=
NM_001301829.1:c.1806G>A	NP_001288758.1:p.Gln602=
NM_001301830.1:c.1581G>A	NP_001288759.1:p.Gln527=
NM_005845.4:c.1806G>A	NP_005836.2:p.Gln602=
XM_005254025.2:c.1677G>A	XP_005254082.1:p.Gln559=
XM_006719914.1:c.1716G>A	XP_006719977.1:p.Gln572=
XM_011521047.1:c.1257G>A	XP_011519349.1:p.Gln419=
XM_017020319.1:c.1677G>A	XP_016875808.1:p.Gln559=
XM_017020320.2:c.1806G>A	XP_016875809.1:p.Gln602=
XM_017020321.1:c.291G>A	XP_016875810.1:p.Gln97=
XM_017020322.1:c.1677G>A	XP_016875811.1:p.Gln559=
NM_001105515.3:c.1806G>A	NP_001098985.1:p.Gln602=
NM_001301829.2:c.1806G>A	NP_001288758.1:p.Gln602=
NM_001301830.2:c.1581G>A	NP_001288759.1:p.Gln527=
NM_005845.5:c.1806G>A MANE Select	NP_005836.2:p.Gln602=