Canonical Allele Identifier: CA2523684112

Gene: ERBB4

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.211377309_211377310insGTTGTCCTTTTCCCTTA , CM000664.2:g.211377309_211377310insGTTGTCCTTTTCCCTTA	GRCh38
NC_000002.11:g.212242034_212242035insGTTGTCCTTTTCCCTTA , CM000664.1:g.212242034_212242035insGTTGTCCTTTTCCCTTA	GRCh37
NC_000002.10:g.211950279_211950280insGTTGTCCTTTTCCCTTA	NCBI36
NG_011805.1:g.1166318_1166319insTAAGGGAAAAGGACAAC
NG_011805.2:g.1166319_1166320insTAAGGGAAAAGGACAAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342788.9:c.*6305_*6306insTAAGGGAAAAGGACAAC MANE Select	ENSP00000342235.4:n.*6305_*6306insTAAGGGAAAAGGACAAC
ENST00000402597.6:c.10106_10107insTAAGGGAAAAGGACAAC	ENSP00000385565.3:n.10106_10107insTAAGGGAAAAGGACAAC
ENST00000342788.8:c.*6305_*6306insTAAGGGAAAAGGACAAC	ENSP00000342235.4:n.*6305_*6306insTAAGGGAAAAGGACAAC
ENST00000402597.5:c.*6305_*6306insTAAGGGAAAAGGACAAC	ENSP00000385565.2:n.*6305_*6306insTAAGGGAAAAGGACAAC
ENST00000436443.5:c.*6305_*6306insTAAGGGAAAAGGACAAC	ENSP00000403204.1:n.*6305_*6306insTAAGGGAAAAGGACAAC
NM_001042599.1:c.*6305_*6306insTAAGGGAAAAGGACAAC	NP_001036064.1:n.*6305_*6306insTAAGGGAAAAGGACAAC
NM_005235.2:c.*6305_*6306insTAAGGGAAAAGGACAAC	NP_005226.1:n.*6305_*6306insTAAGGGAAAAGGACAAC
XM_005246375.1:c.*6305_*6306insTAAGGGAAAAGGACAAC	XP_005246432.1:n.*6305_*6306insTAAGGGAAAAGGACAAC
XM_005246376.1:c.*6305_*6306insTAAGGGAAAAGGACAAC	XP_005246433.1:n.*6305_*6306insTAAGGGAAAAGGACAAC
XM_005246377.1:c.*6305_*6306insTAAGGGAAAAGGACAAC	XP_005246434.1:n.*6305_*6306insTAAGGGAAAAGGACAAC
XM_006712364.1:c.*6305_*6306insTAAGGGAAAAGGACAAC	XP_006712427.1:n.*6305_*6306insTAAGGGAAAAGGACAAC
XM_005246376.3:c.*6305_*6306insTAAGGGAAAAGGACAAC	XP_005246433.1:n.*6305_*6306insTAAGGGAAAAGGACAAC
XM_005246377.3:c.*6305_*6306insTAAGGGAAAAGGACAAC	XP_005246434.1:n.*6305_*6306insTAAGGGAAAAGGACAAC
XM_006712364.3:c.*6305_*6306insTAAGGGAAAAGGACAAC	XP_006712427.1:n.*6305_*6306insTAAGGGAAAAGGACAAC
XM_017003577.2:c.*6305_*6306insTAAGGGAAAAGGACAAC	XP_016859066.1:n.*6305_*6306insTAAGGGAAAAGGACAAC
XM_017003578.2:c.*6305_*6306insTAAGGGAAAAGGACAAC	XP_016859067.1:n.*6305_*6306insTAAGGGAAAAGGACAAC
XM_017003579.2:c.*6305_*6306insTAAGGGAAAAGGACAAC	XP_016859068.1:n.*6305_*6306insTAAGGGAAAAGGACAAC
XM_017003580.2:c.*6305_*6306insTAAGGGAAAAGGACAAC	XP_016859069.1:n.*6305_*6306insTAAGGGAAAAGGACAAC
XM_017003581.2:c.*6305_*6306insTAAGGGAAAAGGACAAC	XP_016859070.1:n.*6305_*6306insTAAGGGAAAAGGACAAC
XM_017003582.1:c.*6305_*6306insTAAGGGAAAAGGACAAC	XP_016859071.1:n.*6305_*6306insTAAGGGAAAAGGACAAC
NM_005235.3:c.*6305_*6306insTAAGGGAAAAGGACAAC MANE Select	NP_005226.1:n.*6305_*6306insTAAGGGAAAAGGACAAC