Canonical Allele Identifier: CA2112099034
Gene: ABCC4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.95061398C= , CM000675.2:g.95061398C= GRCh38
NC_000013.10:g.95713652C= , CM000675.1:g.95713652C= GRCh37
NC_000013.9:g.94511653C= NCBI36
NG_050651.1:g.245049G=
NG_050651.2:g.245049G=

Transcript Alleles

HGVS Amino-acid change
ENST00000643051.1:c.*991+1306G= ENSP00000495513.1:n.*991+1306G=
ENST00000643842.1:c.*3412+1306G= ENSP00000493861.1:n.*3412+1306G=
ENST00000645237.2:c.3366+1306G= MANE Select ENSP00000494609.1:n.3366+1306G=
ENST00000646439.1:c.3225+1306G= ENSP00000494751.1:n.3225+1306G=
ENST00000376887.8:c.3366+1306G= ENSP00000366084.4:n.3366+1306G=
NM_001301829.1:c.3225+1306G= NP_001288758.1:n.3225+1306G=
NM_005845.4:c.3366+1306G= NP_005836.2:n.3366+1306G=
XM_005254025.2:c.3237+1306G= XP_005254082.1:n.3237+1306G=
XM_006719914.1:c.3276+1306G= XP_006719977.1:n.3276+1306G=
XM_011521047.1:c.2817+1306G= XP_011519349.1:n.2817+1306G=
XM_017020319.1:c.3237+1306G= XP_016875808.1:n.3237+1306G=
XM_017020321.1:c.1851+1306G= XP_016875810.1:n.1851+1306G=
NM_001301829.2:c.3225+1306G= NP_001288758.1:n.3225+1306G=
NM_005845.5:c.3366+1306G= MANE Select NP_005836.2:n.3366+1306G=