Canonical Allele Identifier: CA1325614780

Gene: ERBB4

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.211702074G= , CM000664.2:g.211702074G=	GRCh38
NC_000002.11:g.212566799G= , CM000664.1:g.212566799G=	GRCh37
NC_000002.10:g.212275044G=	NCBI36
NG_011805.1:g.841554C=
NG_011805.2:g.841555C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260943.11:c.1382C=	ENSP00000260943.7:p.Thr461=
ENST00000342788.9:c.1382C= MANE Select	ENSP00000342235.4:p.Thr461=
ENST00000402597.6:c.1304C=	ENSP00000385565.3:p.Thr435=
ENST00000260943.10:c.1381C=
ENST00000342788.8:c.1382C=	ENSP00000342235.4:p.Thr461=
ENST00000402597.5:c.1205C=	ENSP00000385565.2:p.Thr402=
ENST00000436443.5:c.1382C=	ENSP00000403204.1:p.Thr461=
ENST00000484594.5:n.1434C=
NM_001042599.1:c.1382C=	NP_001036064.1:p.Thr461=
NM_005235.2:c.1382C=	NP_005226.1:p.Thr461=
XM_005246375.1:c.1382C=	XP_005246432.1:p.Thr461=
XM_005246376.1:c.1382C=	XP_005246433.1:p.Thr461=
XM_005246377.1:c.1382C=	XP_005246434.1:p.Thr461=
XM_006712364.1:c.1382C=	XP_006712427.1:p.Thr461=
XM_005246376.3:c.1382C=	XP_005246433.1:p.Thr461=
XM_005246377.3:c.1382C=	XP_005246434.1:p.Thr461=
XM_006712364.3:c.1382C=	XP_006712427.1:p.Thr461=
XM_017003577.2:c.1460C=	XP_016859066.1:p.Thr487=
XM_017003578.2:c.1460C=	XP_016859067.1:p.Thr487=
XM_017003579.2:c.1460C=	XP_016859068.1:p.Thr487=
XM_017003580.2:c.1460C=	XP_016859069.1:p.Thr487=
XM_017003581.2:c.1460C=	XP_016859070.1:p.Thr487=
XM_017003582.1:c.761C=	XP_016859071.1:p.Thr254=
NM_005235.3:c.1382C= MANE Select	NP_005226.1:p.Thr461=