Canonical Allele Identifier: CA1325972595

Gene: ERBB4

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.212432529G= , CM000664.2:g.212432529G=	GRCh38
NC_000002.11:g.213297253G= , CM000664.1:g.213297253G=	GRCh37
NC_000002.10:g.213005498G=	NCBI36
NG_011805.1:g.111100C=
NG_011805.2:g.111100C=

Transcript Alleles

HGVS	Amino-acid Change
NM_005235.3:c.82+105920C= MANE Select	NP_005226.1:n.82+105920C=
ENST00000342788.9:c.82+105920C= MANE Select	ENSP00000342235.4:n.82+105920C=
NM_001042599.1:c.82+105920C=	NP_001036064.1:n.82+105920C=
NM_005235.2:c.82+105920C=	NP_005226.1:n.82+105920C=
ENST00000260943.10:c.81+105920C=
ENST00000260943.11:c.82+105920C=	ENSP00000260943.7:n.82+105920C=
ENST00000342788.8:c.82+105920C=	ENSP00000342235.4:n.82+105920C=
ENST00000436443.5:c.82+105920C=	ENSP00000403204.1:n.82+105920C=
ENST00000484594.5:n.134+105920C=
XM_005246375.1:c.82+105920C=	XP_005246432.1:n.82+105920C=
XM_005246376.1:c.82+105920C=	XP_005246433.1:n.82+105920C=
XM_005246376.3:c.82+105920C=	XP_005246433.1:n.82+105920C=
XM_005246377.1:c.82+105920C=	XP_005246434.1:n.82+105920C=
XM_005246377.3:c.82+105920C=	XP_005246434.1:n.82+105920C=
XM_006712364.1:c.82+105920C=	XP_006712427.1:n.82+105920C=
XM_006712364.3:c.82+105920C=	XP_006712427.1:n.82+105920C=
XM_017003577.2:c.82+105920C=	XP_016859066.1:n.82+105920C=
XM_017003578.2:c.82+105920C=	XP_016859067.1:n.82+105920C=
XM_017003579.2:c.82+105920C=	XP_016859068.1:n.82+105920C=
XM_017003580.2:c.82+105920C=	XP_016859069.1:n.82+105920C=
XM_017003581.2:c.82+105920C=	XP_016859070.1:n.82+105920C=