Canonical Allele Identifier: CA2087361

Gene: ERBB4

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.211383728C>T , CM000664.2:g.211383728C>T	GRCh38
NC_000002.11:g.212248453C>T , CM000664.1:g.212248453C>T	GRCh37
NC_000002.10:g.211956698C>T	NCBI36
NG_011805.1:g.1159900G>A
NG_011805.2:g.1159901G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_005235.3:c.3814G>A MANE Select	NP_005226.1:p.Gly1272Arg
ENST00000342788.9:c.3814G>A MANE Select	ENSP00000342235.4:p.Gly1272Arg
NM_001042599.1:c.3766G>A	NP_001036064.1:p.Gly1256Arg
NM_005235.2:c.3814G>A	NP_005226.1:p.Gly1272Arg
ENST00000260943.11:c.3736G>A	ENSP00000260943.7:p.Gly1246Arg
ENST00000342788.8:c.3814G>A	ENSP00000342235.4:p.Gly1272Arg
ENST00000402597.5:c.3637G>A	ENSP00000385565.2:p.Gly1213Arg
ENST00000402597.6:c.3688G>A	ENSP00000385565.3:p.Gly1230Arg
ENST00000436443.5:c.3766G>A	ENSP00000403204.1:p.Gly1256Arg
XM_005246375.1:c.3811G>A	XP_005246432.1:p.Gly1271Arg
XM_005246376.1:c.3784G>A	XP_005246433.1:p.Gly1262Arg
XM_005246376.3:c.3784G>A	XP_005246433.1:p.Gly1262Arg
XM_005246377.1:c.3736G>A	XP_005246434.1:p.Gly1246Arg
XM_005246377.3:c.3736G>A	XP_005246434.1:p.Gly1246Arg
XM_006712364.1:c.3859G>A	XP_006712427.1:p.Gly1287Arg
XM_006712364.3:c.3859G>A	XP_006712427.1:p.Gly1287Arg
XM_017003577.2:c.3937G>A	XP_016859066.1:p.Gly1313Arg
XM_017003578.2:c.3892G>A	XP_016859067.1:p.Gly1298Arg
XM_017003579.2:c.3889G>A	XP_016859068.1:p.Gly1297Arg
XM_017003580.2:c.3862G>A	XP_016859069.1:p.Gly1288Arg
XM_017003581.2:c.3844G>A	XP_016859070.1:p.Gly1282Arg
XM_017003582.1:c.3238G>A	XP_016859071.1:p.Gly1080Arg