Canonical Allele Identifier: CA388402939

Gene: ABCC4

Linked Data

• MyVariant Identifiers: chr13:g.95839065A>T (hg19) ; chr13:g.95186811A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.95186811A>T , CM000675.2:g.95186811A>T	GRCh38
NC_000013.10:g.95839065A>T , CM000675.1:g.95839065A>T	GRCh37
NC_000013.9:g.94637066A>T	NCBI36
NG_050651.1:g.119636T>A
NG_050651.2:g.119636T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000642524.1:c.*1468T>A	ENSP00000493766.1:n.*1468T>A
ENST00000643051.1:c.1435T>A	ENSP00000495513.1:p.Ser479Thr
ENST00000643556.1:c.1576T>A	ENSP00000494938.1:n.1576T>A
ENST00000643816.1:n.1718T>A
ENST00000643842.1:c.*1481T>A	ENSP00000493861.1:n.*1481T>A
ENST00000644471.1:n.1531T>A
ENST00000645237.2:c.1435T>A MANE Select	ENSP00000494609.1:p.Ser479Thr
ENST00000645532.1:c.1474T>A	ENSP00000494431.1:p.Ser492Thr
ENST00000646439.1:c.1435T>A	ENSP00000494751.1:p.Ser479Thr
ENST00000376887.8:c.1435T>A	ENSP00000366084.4:p.Ser479Thr
ENST00000536256.3:c.1210T>A	ENSP00000442024.1:p.Ser404Thr
ENST00000629385.1:c.1435T>A	ENSP00000487081.1:p.Ser479Thr
NM_001105515.2:c.1435T>A	NP_001098985.1:p.Ser479Thr
NM_001301829.1:c.1435T>A	NP_001288758.1:p.Ser479Thr
NM_001301830.1:c.1210T>A	NP_001288759.1:p.Ser404Thr
NM_005845.4:c.1435T>A	NP_005836.2:p.Ser479Thr
XM_005254025.2:c.1306T>A	XP_005254082.1:p.Ser436Thr
XM_006719914.1:c.1345T>A	XP_006719977.1:p.Ser449Thr
XM_011521047.1:c.886T>A	XP_011519349.1:p.Ser296Thr
XM_017020319.1:c.1306T>A	XP_016875808.1:p.Ser436Thr
XM_017020320.2:c.1435T>A	XP_016875809.1:p.Ser479Thr
XM_017020322.1:c.1306T>A	XP_016875811.1:p.Ser436Thr
NM_001105515.3:c.1435T>A	NP_001098985.1:p.Ser479Thr
NM_001301829.2:c.1435T>A	NP_001288758.1:p.Ser479Thr
NM_001301830.2:c.1210T>A	NP_001288759.1:p.Ser404Thr
NM_005845.5:c.1435T>A MANE Select	NP_005836.2:p.Ser479Thr