Canonical Allele Identifier: CA1325459941

Gene: ERBB4

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.211377280_211377281delinsAG , CM000664.2:g.211377280_211377281delinsAG	GRCh38
NC_000002.11:g.212242005_212242006delinsAG , CM000664.1:g.212242005_212242006delinsAG	GRCh37
NC_000002.10:g.211950250_211950251delinsAG	NCBI36
NG_011805.1:g.1166347_1166348delinsCT
NG_011805.2:g.1166348_1166349delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342788.9:c.*6334_*6335delinsCT MANE Select	ENSP00000342235.4:n.*6334_*6335delinsCT
ENST00000402597.6:c.10135_10136delinsCT	ENSP00000385565.3:n.10135_10136delinsCT
ENST00000342788.8:c.*6334_*6335delinsCT	ENSP00000342235.4:n.*6334_*6335delinsCT
ENST00000402597.5:c.*6334_*6335delinsCT	ENSP00000385565.2:n.*6334_*6335delinsCT
ENST00000436443.5:c.*6334_*6335delinsCT	ENSP00000403204.1:n.*6334_*6335delinsCT
NM_001042599.1:c.*6334_*6335delinsCT	NP_001036064.1:n.*6334_*6335delinsCT
NM_005235.2:c.*6334_*6335delinsCT	NP_005226.1:n.*6334_*6335delinsCT
XM_005246375.1:c.*6334_*6335delinsCT	XP_005246432.1:n.*6334_*6335delinsCT
XM_005246376.1:c.*6334_*6335delinsCT	XP_005246433.1:n.*6334_*6335delinsCT
XM_005246377.1:c.*6334_*6335delinsCT	XP_005246434.1:n.*6334_*6335delinsCT
XM_006712364.1:c.*6334_*6335delinsCT	XP_006712427.1:n.*6334_*6335delinsCT
XM_005246376.3:c.*6334_*6335delinsCT	XP_005246433.1:n.*6334_*6335delinsCT
XM_005246377.3:c.*6334_*6335delinsCT	XP_005246434.1:n.*6334_*6335delinsCT
XM_006712364.3:c.*6334_*6335delinsCT	XP_006712427.1:n.*6334_*6335delinsCT
XM_017003577.2:c.*6334_*6335delinsCT	XP_016859066.1:n.*6334_*6335delinsCT
XM_017003578.2:c.*6334_*6335delinsCT	XP_016859067.1:n.*6334_*6335delinsCT
XM_017003579.2:c.*6334_*6335delinsCT	XP_016859068.1:n.*6334_*6335delinsCT
XM_017003580.2:c.*6334_*6335delinsCT	XP_016859069.1:n.*6334_*6335delinsCT
XM_017003581.2:c.*6334_*6335delinsCT	XP_016859070.1:n.*6334_*6335delinsCT
XM_017003582.1:c.*6334_*6335delinsCT	XP_016859071.1:n.*6334_*6335delinsCT
NM_005235.3:c.*6334_*6335delinsCT MANE Select	NP_005226.1:n.*6334_*6335delinsCT