Canonical Allele Identifier: CA2087396

Gene: ERBB4

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.211383948G>A , CM000664.2:g.211383948G>A	GRCh38
NC_000002.11:g.212248673G>A , CM000664.1:g.212248673G>A	GRCh37
NC_000002.10:g.211956918G>A	NCBI36
NG_011805.1:g.1159680C>T
NG_011805.2:g.1159681C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_005235.3:c.3594C>T MANE Select	NP_005226.1:p.Ala1198=
ENST00000342788.9:c.3594C>T MANE Select	ENSP00000342235.4:p.Ala1198=
NM_001042599.1:c.3546C>T	NP_001036064.1:p.Ala1182=
NM_005235.2:c.3594C>T	NP_005226.1:p.Ala1198=
ENST00000260943.11:c.3516C>T	ENSP00000260943.7:p.Ala1172=
ENST00000342788.8:c.3594C>T	ENSP00000342235.4:p.Ala1198=
ENST00000402597.5:c.3417C>T	ENSP00000385565.2:p.Ala1139=
ENST00000402597.6:c.3468C>T	ENSP00000385565.3:p.Ala1156=
ENST00000436443.5:c.3546C>T	ENSP00000403204.1:p.Ala1182=
XM_005246375.1:c.3591C>T	XP_005246432.1:p.Ala1197=
XM_005246376.1:c.3564C>T	XP_005246433.1:p.Ala1188=
XM_005246376.3:c.3564C>T	XP_005246433.1:p.Ala1188=
XM_005246377.1:c.3516C>T	XP_005246434.1:p.Ala1172=
XM_005246377.3:c.3516C>T	XP_005246434.1:p.Ala1172=
XM_006712364.1:c.3639C>T	XP_006712427.1:p.Ala1213=
XM_006712364.3:c.3639C>T	XP_006712427.1:p.Ala1213=
XM_017003577.2:c.3717C>T	XP_016859066.1:p.Ala1239=
XM_017003578.2:c.3672C>T	XP_016859067.1:p.Ala1224=
XM_017003579.2:c.3669C>T	XP_016859068.1:p.Ala1223=
XM_017003580.2:c.3642C>T	XP_016859069.1:p.Ala1214=
XM_017003581.2:c.3624C>T	XP_016859070.1:p.Ala1208=
XM_017003582.1:c.3018C>T	XP_016859071.1:p.Ala1006=