Canonical Allele Identifier: CA1325737369
Gene: ERBB4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.211951175_211951190delinsGACTCTTCTTATCAAA , CM000664.2:g.211951175_211951190delinsGACTCTTCTTATCAAA GRCh38
NC_000002.11:g.212815900_212815915delinsGACTCTTCTTATCAAA , CM000664.1:g.212815900_212815915delinsGACTCTTCTTATCAAA GRCh37
NC_000002.10:g.212524145_212524160delinsGACTCTTCTTATCAAA NCBI36
NG_011805.1:g.592438_592453delinsTTTGATAAGAAGAGTC
NG_011805.2:g.592439_592454delinsTTTGATAAGAAGAGTC

Transcript Alleles

HGVS Amino-acid change
ENST00000260943.11:c.235-3574_235-3559delinsTTTGATAAGAAGAGTC ENSP00000260943.7:n.235-3574_235-3559delinsTTTGATAAGAAGAGTC
ENST00000342788.9:c.235-3574_235-3559delinsTTTGATAAGAAGAGTC MANE Select ENSP00000342235.4:n.235-3574_235-3559delinsTTTGATAAGAAGAGTC
ENST00000402597.6:c.157-3574_157-3559delinsTTTGATAAGAAGAGTC ENSP00000385565.3:n.157-3574_157-3559delinsTTTGATAAGAAGAGTC
ENST00000260943.10:c.234-3574_234-3559delinsTTTGATAAGAAGAGTC
ENST00000342788.8:c.235-3574_235-3559delinsTTTGATAAGAAGAGTC ENSP00000342235.4:n.235-3574_235-3559delinsTTTGATAAGAAGAGTC
ENST00000402597.5:c.58-3574_58-3559delinsTTTGATAAGAAGAGTC ENSP00000385565.2:n.58-3574_58-3559delinsTTTGATAAGAAGAGTC
ENST00000435846.1:c.58-3574_58-3559delinsTTTGATAAGAAGAGTC ENSP00000405564.1:n.58-3574_58-3559delinsTTTGATAAGAAGAGTC
ENST00000436443.5:c.235-3574_235-3559delinsTTTGATAAGAAGAGTC ENSP00000403204.1:n.235-3574_235-3559delinsTTTGATAAGAAGAGTC
ENST00000484474.1:n.152-3574_152-3559delinsTTTGATAAGAAGAGTC
ENST00000484594.5:n.287-3574_287-3559delinsTTTGATAAGAAGAGTC
NM_001042599.1:c.235-3574_235-3559delinsTTTGATAAGAAGAGTC NP_001036064.1:n.235-3574_235-3559delinsTTTGATAAGAAGAGTC
NM_005235.2:c.235-3574_235-3559delinsTTTGATAAGAAGAGTC NP_005226.1:n.235-3574_235-3559delinsTTTGATAAGAAGAGTC
XM_005246375.1:c.235-3574_235-3559delinsTTTGATAAGAAGAGTC XP_005246432.1:n.235-3574_235-3559delinsTTTGATAAGAAGAGTC
XM_005246376.1:c.235-3574_235-3559delinsTTTGATAAGAAGAGTC XP_005246433.1:n.235-3574_235-3559delinsTTTGATAAGAAGAGTC
XM_005246377.1:c.235-3574_235-3559delinsTTTGATAAGAAGAGTC XP_005246434.1:n.235-3574_235-3559delinsTTTGATAAGAAGAGTC
XM_006712364.1:c.235-3574_235-3559delinsTTTGATAAGAAGAGTC XP_006712427.1:n.235-3574_235-3559delinsTTTGATAAGAAGAGTC
XM_005246376.3:c.235-3574_235-3559delinsTTTGATAAGAAGAGTC XP_005246433.1:n.235-3574_235-3559delinsTTTGATAAGAAGAGTC
XM_005246377.3:c.235-3574_235-3559delinsTTTGATAAGAAGAGTC XP_005246434.1:n.235-3574_235-3559delinsTTTGATAAGAAGAGTC
XM_006712364.3:c.235-3574_235-3559delinsTTTGATAAGAAGAGTC XP_006712427.1:n.235-3574_235-3559delinsTTTGATAAGAAGAGTC
XM_017003577.2:c.235-3574_235-3559delinsTTTGATAAGAAGAGTC XP_016859066.1:n.235-3574_235-3559delinsTTTGATAAGAAGAGTC
XM_017003578.2:c.235-3574_235-3559delinsTTTGATAAGAAGAGTC XP_016859067.1:n.235-3574_235-3559delinsTTTGATAAGAAGAGTC
XM_017003579.2:c.235-3574_235-3559delinsTTTGATAAGAAGAGTC XP_016859068.1:n.235-3574_235-3559delinsTTTGATAAGAAGAGTC
XM_017003580.2:c.235-3574_235-3559delinsTTTGATAAGAAGAGTC XP_016859069.1:n.235-3574_235-3559delinsTTTGATAAGAAGAGTC
XM_017003581.2:c.235-3574_235-3559delinsTTTGATAAGAAGAGTC XP_016859070.1:n.235-3574_235-3559delinsTTTGATAAGAAGAGTC
NM_005235.3:c.235-3574_235-3559delinsTTTGATAAGAAGAGTC MANE Select NP_005226.1:n.235-3574_235-3559delinsTTTGATAAGAAGAGTC