Canonical Allele Identifier: CA388403020

Gene: ABCC4

Linked Data

• MyVariant Identifiers: chr13:g.95839085T>G (hg19) ; chr13:g.95186831T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.95186831T>G , CM000675.2:g.95186831T>G	GRCh38
NC_000013.10:g.95839085T>G , CM000675.1:g.95839085T>G	GRCh37
NC_000013.9:g.94637086T>G	NCBI36
NG_050651.1:g.119616A>C
NG_050651.2:g.119616A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642524.1:c.*1448A>C	ENSP00000493766.1:n.*1448A>C
ENST00000643051.1:c.1415A>C	ENSP00000495513.1:p.His472Pro
ENST00000643556.1:c.1556A>C	ENSP00000494938.1:n.1556A>C
ENST00000643816.1:n.1698A>C
ENST00000643842.1:c.*1461A>C	ENSP00000493861.1:n.*1461A>C
ENST00000644471.1:n.1511A>C
ENST00000645237.2:c.1415A>C MANE Select	ENSP00000494609.1:p.His472Pro
ENST00000645532.1:c.1454A>C	ENSP00000494431.1:p.His485Pro
ENST00000646439.1:c.1415A>C	ENSP00000494751.1:p.His472Pro
ENST00000376887.8:c.1415A>C	ENSP00000366084.4:p.His472Pro
ENST00000536256.3:c.1190A>C	ENSP00000442024.1:p.His397Pro
ENST00000629385.1:c.1415A>C	ENSP00000487081.1:p.His472Pro
NM_001105515.2:c.1415A>C	NP_001098985.1:p.His472Pro
NM_001301829.1:c.1415A>C	NP_001288758.1:p.His472Pro
NM_001301830.1:c.1190A>C	NP_001288759.1:p.His397Pro
NM_005845.4:c.1415A>C	NP_005836.2:p.His472Pro
XM_005254025.2:c.1286A>C	XP_005254082.1:p.His429Pro
XM_006719914.1:c.1325A>C	XP_006719977.1:p.His442Pro
XM_011521047.1:c.866A>C	XP_011519349.1:p.His289Pro
XM_017020319.1:c.1286A>C	XP_016875808.1:p.His429Pro
XM_017020320.2:c.1415A>C	XP_016875809.1:p.His472Pro
XM_017020322.1:c.1286A>C	XP_016875811.1:p.His429Pro
NM_001105515.3:c.1415A>C	NP_001098985.1:p.His472Pro
NM_001301829.2:c.1415A>C	NP_001288758.1:p.His472Pro
NM_001301830.2:c.1190A>C	NP_001288759.1:p.His397Pro
NM_005845.5:c.1415A>C MANE Select	NP_005836.2:p.His472Pro