Canonical Allele Identifier: CA2088466

Gene: ERBB4

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.211947543C>T , CM000664.2:g.211947543C>T	GRCh38
NC_000002.11:g.212812268C>T , CM000664.1:g.212812268C>T	GRCh37
NC_000002.10:g.212520513C>T	NCBI36
NG_011805.1:g.596085G>A
NG_011805.2:g.596086G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_005235.3:c.308G>A MANE Select	NP_005226.1:p.Arg103His
ENST00000342788.9:c.308G>A MANE Select	ENSP00000342235.4:p.Arg103His
NM_001042599.1:c.308G>A	NP_001036064.1:p.Arg103His
NM_005235.2:c.308G>A	NP_005226.1:p.Arg103His
ENST00000260943.10:c.307G>A
ENST00000260943.11:c.308G>A	ENSP00000260943.7:p.Arg103His
ENST00000342788.8:c.308G>A	ENSP00000342235.4:p.Arg103His
ENST00000402597.5:c.131G>A	ENSP00000385565.2:p.Arg44His
ENST00000402597.6:c.230G>A	ENSP00000385565.3:p.Arg77His
ENST00000435846.1:c.131G>A	ENSP00000405564.1:p.Arg44His
ENST00000436443.5:c.308G>A	ENSP00000403204.1:p.Arg103His
ENST00000484474.1:n.225G>A
ENST00000484594.5:n.360G>A
XM_005246375.1:c.308G>A	XP_005246432.1:p.Arg103His
XM_005246376.1:c.308G>A	XP_005246433.1:p.Arg103His
XM_005246376.3:c.308G>A	XP_005246433.1:p.Arg103His
XM_005246377.1:c.308G>A	XP_005246434.1:p.Arg103His
XM_005246377.3:c.308G>A	XP_005246434.1:p.Arg103His
XM_006712364.1:c.308G>A	XP_006712427.1:p.Arg103His
XM_006712364.3:c.308G>A	XP_006712427.1:p.Arg103His
XM_017003577.2:c.308G>A	XP_016859066.1:p.Arg103His
XM_017003578.2:c.308G>A	XP_016859067.1:p.Arg103His
XM_017003579.2:c.308G>A	XP_016859068.1:p.Arg103His
XM_017003580.2:c.308G>A	XP_016859069.1:p.Arg103His
XM_017003581.2:c.308G>A	XP_016859070.1:p.Arg103His