Canonical Allele Identifier: CA2577232945

Gene: ERBB4

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.211702185_211702186del , CM000664.2:g.211702185_211702186del	GRCh38
NC_000002.11:g.212566910_212566911del , CM000664.1:g.212566910_212566911del	GRCh37
NC_000002.10:g.212275155_212275156del	NCBI36
NG_011805.1:g.841444_841445del
NG_011805.2:g.841445_841446del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260943.11:c.1290-18_1290-17del	ENSP00000260943.7:n.1290-18_1290-17del
ENST00000342788.9:c.1290-18_1290-17del MANE Select	ENSP00000342235.4:n.1290-18_1290-17del
ENST00000402597.6:c.1212-18_1212-17del	ENSP00000385565.3:n.1212-18_1212-17del
ENST00000260943.10:c.1289-18_1289-17del
ENST00000342788.8:c.1290-18_1290-17del	ENSP00000342235.4:n.1290-18_1290-17del
ENST00000402597.5:c.1113-18_1113-17del	ENSP00000385565.2:n.1113-18_1113-17del
ENST00000436443.5:c.1290-18_1290-17del	ENSP00000403204.1:n.1290-18_1290-17del
ENST00000484594.5:n.1342-18_1342-17del
NM_001042599.1:c.1290-18_1290-17del	NP_001036064.1:n.1290-18_1290-17del
NM_005235.2:c.1290-18_1290-17del	NP_005226.1:n.1290-18_1290-17del
XM_005246375.1:c.1290-18_1290-17del	XP_005246432.1:n.1290-18_1290-17del
XM_005246376.1:c.1290-18_1290-17del	XP_005246433.1:n.1290-18_1290-17del
XM_005246377.1:c.1290-18_1290-17del	XP_005246434.1:n.1290-18_1290-17del
XM_006712364.1:c.1290-18_1290-17del	XP_006712427.1:n.1290-18_1290-17del
XM_005246376.3:c.1290-18_1290-17del	XP_005246433.1:n.1290-18_1290-17del
XM_005246377.3:c.1290-18_1290-17del	XP_005246434.1:n.1290-18_1290-17del
XM_006712364.3:c.1290-18_1290-17del	XP_006712427.1:n.1290-18_1290-17del
XM_017003577.2:c.1368-18_1368-17del	XP_016859066.1:n.1368-18_1368-17del
XM_017003578.2:c.1368-18_1368-17del	XP_016859067.1:n.1368-18_1368-17del
XM_017003579.2:c.1368-18_1368-17del	XP_016859068.1:n.1368-18_1368-17del
XM_017003580.2:c.1368-18_1368-17del	XP_016859069.1:n.1368-18_1368-17del
XM_017003581.2:c.1368-18_1368-17del	XP_016859070.1:n.1368-18_1368-17del
XM_017003582.1:c.669-18_669-17del	XP_016859071.1:n.669-18_669-17del
NM_005235.3:c.1290-18_1290-17del MANE Select	NP_005226.1:n.1290-18_1290-17del