Canonical Allele Identifier: CA431125265

Gene: ERBB4

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.211383969T>A , CM000664.2:g.211383969T>A	GRCh38
NC_000002.11:g.212248694T>A , CM000664.1:g.212248694T>A	GRCh37
NC_000002.10:g.211956939T>A	NCBI36
NG_011805.1:g.1159659A>T
NG_011805.2:g.1159660A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_005235.3:c.3573A>T MANE Select	NP_005226.1:p.Ala1191=
ENST00000342788.9:c.3573A>T MANE Select	ENSP00000342235.4:p.Ala1191=
NM_001042599.1:c.3525A>T	NP_001036064.1:p.Ala1175=
NM_005235.2:c.3573A>T	NP_005226.1:p.Ala1191=
ENST00000260943.11:c.3495A>T	ENSP00000260943.7:p.Ala1165=
ENST00000342788.8:c.3573A>T	ENSP00000342235.4:p.Ala1191=
ENST00000402597.5:c.3396A>T	ENSP00000385565.2:p.Ala1132=
ENST00000402597.6:c.3447A>T	ENSP00000385565.3:p.Ala1149=
ENST00000436443.5:c.3525A>T	ENSP00000403204.1:p.Ala1175=
XM_005246375.1:c.3570A>T	XP_005246432.1:p.Ala1190=
XM_005246376.1:c.3543A>T	XP_005246433.1:p.Ala1181=
XM_005246376.3:c.3543A>T	XP_005246433.1:p.Ala1181=
XM_005246377.1:c.3495A>T	XP_005246434.1:p.Ala1165=
XM_005246377.3:c.3495A>T	XP_005246434.1:p.Ala1165=
XM_006712364.1:c.3618A>T	XP_006712427.1:p.Ala1206=
XM_006712364.3:c.3618A>T	XP_006712427.1:p.Ala1206=
XM_017003577.2:c.3696A>T	XP_016859066.1:p.Ala1232=
XM_017003578.2:c.3651A>T	XP_016859067.1:p.Ala1217=
XM_017003579.2:c.3648A>T	XP_016859068.1:p.Ala1216=
XM_017003580.2:c.3621A>T	XP_016859069.1:p.Ala1207=
XM_017003581.2:c.3603A>T	XP_016859070.1:p.Ala1201=
XM_017003582.1:c.2997A>T	XP_016859071.1:p.Ala999=