Canonical Allele Identifier: CA388402978

Gene: ABCC4

Linked Data

• MyVariant Identifiers: chr13:g.95839075A>C (hg19) ; chr13:g.95186821A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.95186821A>C , CM000675.2:g.95186821A>C	GRCh38
NC_000013.10:g.95839075A>C , CM000675.1:g.95839075A>C	GRCh37
NC_000013.9:g.94637076A>C	NCBI36
NG_050651.1:g.119626T>G
NG_050651.2:g.119626T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642524.1:c.*1458T>G	ENSP00000493766.1:n.*1458T>G
ENST00000643051.1:c.1425T>G	ENSP00000495513.1:p.Ile475Met
ENST00000643556.1:c.1566T>G	ENSP00000494938.1:n.1566T>G
ENST00000643816.1:n.1708T>G
ENST00000643842.1:c.*1471T>G	ENSP00000493861.1:n.*1471T>G
ENST00000644471.1:n.1521T>G
ENST00000645237.2:c.1425T>G MANE Select	ENSP00000494609.1:p.Ile475Met
ENST00000645532.1:c.1464T>G	ENSP00000494431.1:p.Ile488Met
ENST00000646439.1:c.1425T>G	ENSP00000494751.1:p.Ile475Met
ENST00000376887.8:c.1425T>G	ENSP00000366084.4:p.Ile475Met
ENST00000536256.3:c.1200T>G	ENSP00000442024.1:p.Ile400Met
ENST00000629385.1:c.1425T>G	ENSP00000487081.1:p.Ile475Met
NM_001105515.2:c.1425T>G	NP_001098985.1:p.Ile475Met
NM_001301829.1:c.1425T>G	NP_001288758.1:p.Ile475Met
NM_001301830.1:c.1200T>G	NP_001288759.1:p.Ile400Met
NM_005845.4:c.1425T>G	NP_005836.2:p.Ile475Met
XM_005254025.2:c.1296T>G	XP_005254082.1:p.Ile432Met
XM_006719914.1:c.1335T>G	XP_006719977.1:p.Ile445Met
XM_011521047.1:c.876T>G	XP_011519349.1:p.Ile292Met
XM_017020319.1:c.1296T>G	XP_016875808.1:p.Ile432Met
XM_017020320.2:c.1425T>G	XP_016875809.1:p.Ile475Met
XM_017020322.1:c.1296T>G	XP_016875811.1:p.Ile432Met
NM_001105515.3:c.1425T>G	NP_001098985.1:p.Ile475Met
NM_001301829.2:c.1425T>G	NP_001288758.1:p.Ile475Met
NM_001301830.2:c.1200T>G	NP_001288759.1:p.Ile400Met
NM_005845.5:c.1425T>G MANE Select	NP_005836.2:p.Ile475Met