Canonical Allele Identifier: CA1325462853

Gene: ERBB4

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.211383719G= , CM000664.2:g.211383719G=	GRCh38
NC_000002.11:g.212248444G= , CM000664.1:g.212248444G=	GRCh37
NC_000002.10:g.211956689G=	NCBI36
NG_011805.1:g.1159909C=
NG_011805.2:g.1159910C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260943.11:c.3745C=	ENSP00000260943.7:p.Arg1249=
ENST00000342788.9:c.3823C= MANE Select	ENSP00000342235.4:p.Arg1275=
ENST00000402597.6:c.3697C=	ENSP00000385565.3:p.Arg1233=
ENST00000342788.8:c.3823C=	ENSP00000342235.4:p.Arg1275=
ENST00000402597.5:c.3646C=	ENSP00000385565.2:p.Arg1216=
ENST00000436443.5:c.3775C=	ENSP00000403204.1:p.Arg1259=
NM_001042599.1:c.3775C=	NP_001036064.1:p.Arg1259=
NM_005235.2:c.3823C=	NP_005226.1:p.Arg1275=
XM_005246375.1:c.3820C=	XP_005246432.1:p.Arg1274=
XM_005246376.1:c.3793C=	XP_005246433.1:p.Arg1265=
XM_005246377.1:c.3745C=	XP_005246434.1:p.Arg1249=
XM_006712364.1:c.3868C=	XP_006712427.1:p.Arg1290=
XM_005246376.3:c.3793C=	XP_005246433.1:p.Arg1265=
XM_005246377.3:c.3745C=	XP_005246434.1:p.Arg1249=
XM_006712364.3:c.3868C=	XP_006712427.1:p.Arg1290=
XM_017003577.2:c.3946C=	XP_016859066.1:p.Arg1316=
XM_017003578.2:c.3901C=	XP_016859067.1:p.Arg1301=
XM_017003579.2:c.3898C=	XP_016859068.1:p.Arg1300=
XM_017003580.2:c.3871C=	XP_016859069.1:p.Arg1291=
XM_017003581.2:c.3853C=	XP_016859070.1:p.Arg1285=
XM_017003582.1:c.3247C=	XP_016859071.1:p.Arg1083=
NM_005235.3:c.3823C= MANE Select	NP_005226.1:p.Arg1275=