Canonical Allele Identifier: CA2087439

Gene: ERBB4

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.211386888C>A , CM000664.2:g.211386888C>A	GRCh38
NC_000002.11:g.212251613C>A , CM000664.1:g.212251613C>A	GRCh37
NC_000002.10:g.211959858C>A	NCBI36
NG_011805.1:g.1156740G>T
NG_011805.2:g.1156741G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_005235.3:c.3446G>T MANE Select	NP_005226.1:p.Gly1149Val
ENST00000342788.9:c.3446G>T MANE Select	ENSP00000342235.4:p.Gly1149Val
NM_001042599.1:c.3398G>T	NP_001036064.1:p.Gly1133Val
NM_005235.2:c.3446G>T	NP_005226.1:p.Gly1149Val
ENST00000260943.11:c.3368G>T	ENSP00000260943.7:p.Gly1123Val
ENST00000342788.8:c.3446G>T	ENSP00000342235.4:p.Gly1149Val
ENST00000402597.5:c.3269G>T	ENSP00000385565.2:p.Gly1090Val
ENST00000402597.6:c.3320G>T	ENSP00000385565.3:p.Gly1107Val
ENST00000436443.5:c.3398G>T	ENSP00000403204.1:p.Gly1133Val
XM_005246375.1:c.3443G>T	XP_005246432.1:p.Gly1148Val
XM_005246376.1:c.3416G>T	XP_005246433.1:p.Gly1139Val
XM_005246376.3:c.3416G>T	XP_005246433.1:p.Gly1139Val
XM_005246377.1:c.3368G>T	XP_005246434.1:p.Gly1123Val
XM_005246377.3:c.3368G>T	XP_005246434.1:p.Gly1123Val
XM_006712364.1:c.3491G>T	XP_006712427.1:p.Gly1164Val
XM_006712364.3:c.3491G>T	XP_006712427.1:p.Gly1164Val
XM_017003577.2:c.3569G>T	XP_016859066.1:p.Gly1190Val
XM_017003578.2:c.3524G>T	XP_016859067.1:p.Gly1175Val
XM_017003579.2:c.3521G>T	XP_016859068.1:p.Gly1174Val
XM_017003580.2:c.3494G>T	XP_016859069.1:p.Gly1165Val
XM_017003581.2:c.3476G>T	XP_016859070.1:p.Gly1159Val
XM_017003582.1:c.2870G>T	XP_016859071.1:p.Gly957Val