Canonical Allele Identifier: CA484497980

Gene: ABCC4

Linked Data

• MyVariant Identifiers: chr13:g.95838964A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.95186710A>G , CM000675.2:g.95186710A>G	GRCh38
NC_000013.10:g.95838964A>G , CM000675.1:g.95838964A>G	GRCh37
NC_000013.9:g.94636965A>G	NCBI36
NG_050651.1:g.119737T>C
NG_050651.2:g.119737T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000642524.1:c.*1569T>C	ENSP00000493766.1:n.*1569T>C
ENST00000643051.1:c.1536T>C	ENSP00000495513.1:p.Ala512=
ENST00000643556.1:c.1677T>C	ENSP00000494938.1:n.1677T>C
ENST00000643816.1:n.1819T>C
ENST00000643842.1:c.*1582T>C	ENSP00000493861.1:n.*1582T>C
ENST00000644471.1:n.1632T>C
ENST00000645237.2:c.1536T>C MANE Select	ENSP00000494609.1:p.Ala512=
ENST00000645532.1:c.1575T>C	ENSP00000494431.1:p.Ala525=
ENST00000646439.1:c.1536T>C	ENSP00000494751.1:p.Ala512=
ENST00000376887.8:c.1536T>C	ENSP00000366084.4:p.Ala512=
ENST00000536256.3:c.1311T>C	ENSP00000442024.1:p.Ala437=
ENST00000629385.1:c.1536T>C	ENSP00000487081.1:p.Ala512=
NM_001105515.2:c.1536T>C	NP_001098985.1:p.Ala512=
NM_001301829.1:c.1536T>C	NP_001288758.1:p.Ala512=
NM_001301830.1:c.1311T>C	NP_001288759.1:p.Ala437=
NM_005845.4:c.1536T>C	NP_005836.2:p.Ala512=
XM_005254025.2:c.1407T>C	XP_005254082.1:p.Ala469=
XM_006719914.1:c.1446T>C	XP_006719977.1:p.Ala482=
XM_011521047.1:c.987T>C	XP_011519349.1:p.Ala329=
XM_017020319.1:c.1407T>C	XP_016875808.1:p.Ala469=
XM_017020320.2:c.1536T>C	XP_016875809.1:p.Ala512=
XM_017020322.1:c.1407T>C	XP_016875811.1:p.Ala469=
NM_001105515.3:c.1536T>C	NP_001098985.1:p.Ala512=
NM_001301829.2:c.1536T>C	NP_001288758.1:p.Ala512=
NM_001301830.2:c.1311T>C	NP_001288759.1:p.Ala437=
NM_005845.5:c.1536T>C MANE Select	NP_005836.2:p.Ala512=