Canonical Allele Identifier: CA1325482406

Gene: ERBB4

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.211424241C= , CM000664.2:g.211424241C=	GRCh38
NC_000002.11:g.212288966C= , CM000664.1:g.212288966C=	GRCh37
NC_000002.10:g.211997211C=	NCBI36
NG_011805.1:g.1119387G=
NG_011805.2:g.1119388G=

Transcript Alleles

HGVS	Amino-acid Change
NM_005235.3:c.2780G= MANE Select	NP_005226.1:p.Arg927=
ENST00000342788.9:c.2780G= MANE Select	ENSP00000342235.4:p.Arg927=
NM_001042599.1:c.2780G=	NP_001036064.1:p.Arg927=
NM_005235.2:c.2780G=	NP_005226.1:p.Arg927=
ENST00000260943.11:c.2750G=	ENSP00000260943.7:p.Arg917=
ENST00000342788.8:c.2780G=	ENSP00000342235.4:p.Arg927=
ENST00000402597.5:c.2603G=	ENSP00000385565.2:p.Arg868=
ENST00000402597.6:c.2702G=	ENSP00000385565.3:p.Arg901=
ENST00000436443.5:c.2780G=	ENSP00000403204.1:p.Arg927=
XM_005246375.1:c.2825G=	XP_005246432.1:p.Arg942=
XM_005246376.1:c.2750G=	XP_005246433.1:p.Arg917=
XM_005246376.3:c.2750G=	XP_005246433.1:p.Arg917=
XM_005246377.1:c.2750G=	XP_005246434.1:p.Arg917=
XM_005246377.3:c.2750G=	XP_005246434.1:p.Arg917=
XM_006712364.1:c.2825G=	XP_006712427.1:p.Arg942=
XM_006712364.3:c.2825G=	XP_006712427.1:p.Arg942=
XM_017003577.2:c.2903G=	XP_016859066.1:p.Arg968=
XM_017003578.2:c.2858G=	XP_016859067.1:p.Arg953=
XM_017003579.2:c.2903G=	XP_016859068.1:p.Arg968=
XM_017003580.2:c.2828G=	XP_016859069.1:p.Arg943=
XM_017003581.2:c.2858G=	XP_016859070.1:p.Arg953=
XM_017003582.1:c.2204G=	XP_016859071.1:p.Arg735=