Canonical Allele Identifier: CA1325464386

Gene: ERBB4

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.211387139T= , CM000664.2:g.211387139T=	GRCh38
NC_000002.11:g.212251864T= , CM000664.1:g.212251864T=	GRCh37
NC_000002.10:g.211960109T=	NCBI36
NG_011805.1:g.1156489A=
NG_011805.2:g.1156490A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260943.11:c.3117A=	ENSP00000260943.7:p.Val1039=
ENST00000342788.9:c.3195A= MANE Select	ENSP00000342235.4:p.Val1065=
ENST00000402597.6:c.3069A=	ENSP00000385565.3:p.Val1023=
ENST00000342788.8:c.3195A=	ENSP00000342235.4:p.Val1065=
ENST00000402597.5:c.3018A=	ENSP00000385565.2:p.Val1006=
ENST00000436443.5:c.3147A=	ENSP00000403204.1:p.Val1049=
NM_001042599.1:c.3147A=	NP_001036064.1:p.Val1049=
NM_005235.2:c.3195A=	NP_005226.1:p.Val1065=
XM_005246375.1:c.3192A=	XP_005246432.1:p.Val1064=
XM_005246376.1:c.3165A=	XP_005246433.1:p.Val1055=
XM_005246377.1:c.3117A=	XP_005246434.1:p.Val1039=
XM_006712364.1:c.3240A=	XP_006712427.1:p.Val1080=
XM_005246376.3:c.3165A=	XP_005246433.1:p.Val1055=
XM_005246377.3:c.3117A=	XP_005246434.1:p.Val1039=
XM_006712364.3:c.3240A=	XP_006712427.1:p.Val1080=
XM_017003577.2:c.3318A=	XP_016859066.1:p.Val1106=
XM_017003578.2:c.3273A=	XP_016859067.1:p.Val1091=
XM_017003579.2:c.3270A=	XP_016859068.1:p.Val1090=
XM_017003580.2:c.3243A=	XP_016859069.1:p.Val1081=
XM_017003581.2:c.3225A=	XP_016859070.1:p.Val1075=
XM_017003582.1:c.2619A=	XP_016859071.1:p.Val873=
NM_005235.3:c.3195A= MANE Select	NP_005226.1:p.Val1065=