Canonical Allele Identifier: CA388400315

Gene: ABCC4

Linked Data

• gnomAD v4: 13-95170609-G-A
• MyVariant Identifiers: chr13:g.95822863G>A (hg19) ; chr13:g.95170609G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.95170609G>A , CM000675.2:g.95170609G>A	GRCh38
NC_000013.10:g.95822863G>A , CM000675.1:g.95822863G>A	GRCh37
NC_000013.9:g.94620864G>A	NCBI36
NG_050651.1:g.135838C>T
NG_050651.2:g.135838C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642524.1:c.*1780C>T	ENSP00000493766.1:n.*1780C>T
ENST00000643051.1:c.1747C>T	ENSP00000495513.1:p.His583Tyr
ENST00000643556.1:c.1888C>T	ENSP00000494938.1:n.1888C>T
ENST00000643816.1:n.2030C>T
ENST00000643842.1:c.*1793C>T	ENSP00000493861.1:n.*1793C>T
ENST00000644471.1:n.1838C>T
ENST00000645237.2:c.1747C>T MANE Select	ENSP00000494609.1:p.His583Tyr
ENST00000645532.1:c.1786C>T	ENSP00000494431.1:p.His596Tyr
ENST00000646439.1:c.1747C>T	ENSP00000494751.1:p.His583Tyr
ENST00000376887.8:c.1747C>T	ENSP00000366084.4:p.His583Tyr
ENST00000536256.3:c.1522C>T	ENSP00000442024.1:p.His508Tyr
ENST00000629385.1:c.1747C>T	ENSP00000487081.1:p.His583Tyr
NM_001105515.2:c.1747C>T	NP_001098985.1:p.His583Tyr
NM_001301829.1:c.1747C>T	NP_001288758.1:p.His583Tyr
NM_001301830.1:c.1522C>T	NP_001288759.1:p.His508Tyr
NM_005845.4:c.1747C>T	NP_005836.2:p.His583Tyr
XM_005254025.2:c.1618C>T	XP_005254082.1:p.His540Tyr
XM_006719914.1:c.1657C>T	XP_006719977.1:p.His553Tyr
XM_011521047.1:c.1198C>T	XP_011519349.1:p.His400Tyr
XM_017020319.1:c.1618C>T	XP_016875808.1:p.His540Tyr
XM_017020320.2:c.1747C>T	XP_016875809.1:p.His583Tyr
XM_017020321.1:c.232C>T	XP_016875810.1:p.His78Tyr
XM_017020322.1:c.1618C>T	XP_016875811.1:p.His540Tyr
NM_001105515.3:c.1747C>T	NP_001098985.1:p.His583Tyr
NM_001301829.2:c.1747C>T	NP_001288758.1:p.His583Tyr
NM_001301830.2:c.1522C>T	NP_001288759.1:p.His508Tyr
NM_005845.5:c.1747C>T MANE Select	NP_005836.2:p.His583Tyr