Canonical Allele Identifier: CA431125409

Gene: ERBB4

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.211383807G>A , CM000664.2:g.211383807G>A	GRCh38
NC_000002.11:g.212248532G>A , CM000664.1:g.212248532G>A	GRCh37
NC_000002.10:g.211956777G>A	NCBI36
NG_011805.1:g.1159821C>T
NG_011805.2:g.1159822C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_005235.3:c.3735C>T MANE Select	NP_005226.1:p.His1245=
ENST00000342788.9:c.3735C>T MANE Select	ENSP00000342235.4:p.His1245=
NM_001042599.1:c.3687C>T	NP_001036064.1:p.His1229=
NM_005235.2:c.3735C>T	NP_005226.1:p.His1245=
ENST00000260943.11:c.3657C>T	ENSP00000260943.7:p.His1219=
ENST00000342788.8:c.3735C>T	ENSP00000342235.4:p.His1245=
ENST00000402597.5:c.3558C>T	ENSP00000385565.2:p.His1186=
ENST00000402597.6:c.3609C>T	ENSP00000385565.3:p.His1203=
ENST00000436443.5:c.3687C>T	ENSP00000403204.1:p.His1229=
XM_005246375.1:c.3732C>T	XP_005246432.1:p.His1244=
XM_005246376.1:c.3705C>T	XP_005246433.1:p.His1235=
XM_005246376.3:c.3705C>T	XP_005246433.1:p.His1235=
XM_005246377.1:c.3657C>T	XP_005246434.1:p.His1219=
XM_005246377.3:c.3657C>T	XP_005246434.1:p.His1219=
XM_006712364.1:c.3780C>T	XP_006712427.1:p.His1260=
XM_006712364.3:c.3780C>T	XP_006712427.1:p.His1260=
XM_017003577.2:c.3858C>T	XP_016859066.1:p.His1286=
XM_017003578.2:c.3813C>T	XP_016859067.1:p.His1271=
XM_017003579.2:c.3810C>T	XP_016859068.1:p.His1270=
XM_017003580.2:c.3783C>T	XP_016859069.1:p.His1261=
XM_017003581.2:c.3765C>T	XP_016859070.1:p.His1255=
XM_017003582.1:c.3159C>T	XP_016859071.1:p.His1053=