Canonical Allele Identifier: CA2112112139

Gene: ABCC4

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.95170511A= , CM000675.2:g.95170511A=	GRCh38
NC_000013.10:g.95822765A= , CM000675.1:g.95822765A=	GRCh37
NC_000013.9:g.94620766A=	NCBI36
NG_050651.1:g.135936T=
NG_050651.2:g.135936T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642524.1:c.*1857+21T=	ENSP00000493766.1:n.*1857+21T=
ENST00000643051.1:c.1824+21T=	ENSP00000495513.1:n.1824+21T=
ENST00000643556.1:c.1965+21T=	ENSP00000494938.1:n.1965+21T=
ENST00000643816.1:n.2107+21T=
ENST00000643842.1:c.*1870+21T=	ENSP00000493861.1:n.*1870+21T=
ENST00000644471.1:n.1936T=
ENST00000645237.2:c.1824+21T= MANE Select	ENSP00000494609.1:n.1824+21T=
ENST00000645532.1:c.1863+21T=	ENSP00000494431.1:n.1863+21T=
ENST00000646439.1:c.1824+21T=	ENSP00000494751.1:n.1824+21T=
ENST00000376887.8:c.1824+21T=	ENSP00000366084.4:n.1824+21T=
ENST00000536256.3:c.1599+21T=	ENSP00000442024.1:n.1599+21T=
ENST00000629385.1:c.1824+21T=	ENSP00000487081.1:n.1824+21T=
NM_001105515.2:c.1824+21T=	NP_001098985.1:n.1824+21T=
NM_001301829.1:c.1824+21T=	NP_001288758.1:n.1824+21T=
NM_001301830.1:c.1599+21T=	NP_001288759.1:n.1599+21T=
NM_005845.4:c.1824+21T=	NP_005836.2:n.1824+21T=
XM_005254025.2:c.1695+21T=	XP_005254082.1:n.1695+21T=
XM_006719914.1:c.1734+21T=	XP_006719977.1:n.1734+21T=
XM_011521047.1:c.1275+21T=	XP_011519349.1:n.1275+21T=
XM_017020319.1:c.1695+21T=	XP_016875808.1:n.1695+21T=
XM_017020320.2:c.1824+21T=	XP_016875809.1:n.1824+21T=
XM_017020321.1:c.309+21T=	XP_016875810.1:n.309+21T=
XM_017020322.1:c.1695+21T=	XP_016875811.1:n.1695+21T=
NM_001105515.3:c.1824+21T=	NP_001098985.1:n.1824+21T=
NM_001301829.2:c.1824+21T=	NP_001288758.1:n.1824+21T=
NM_001301830.2:c.1599+21T=	NP_001288759.1:n.1599+21T=
NM_005845.5:c.1824+21T= MANE Select	NP_005836.2:n.1824+21T=