Canonical Allele Identifier: CA1325614815

Gene: ERBB4

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.211702168_211702171delinsTAAG , CM000664.2:g.211702168_211702171delinsTAAG	GRCh38
NC_000002.11:g.212566893_212566896delinsTAAG , CM000664.1:g.212566893_212566896delinsTAAG	GRCh37
NC_000002.10:g.212275138_212275141delinsTAAG	NCBI36
NG_011805.1:g.841457_841460delinsCTTA
NG_011805.2:g.841458_841461delinsCTTA

Transcript Alleles

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