Canonical Allele Identifier: CA1325737375
Gene: ERBB4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.211951187_211951188delinsCA , CM000664.2:g.211951187_211951188delinsCA GRCh38
NC_000002.11:g.212815912_212815913delinsCA , CM000664.1:g.212815912_212815913delinsCA GRCh37
NC_000002.10:g.212524157_212524158delinsCA NCBI36
NG_011805.1:g.592440_592441delinsTG
NG_011805.2:g.592441_592442delinsTG

Transcript Alleles

HGVS Amino-acid change
ENST00000260943.11:c.235-3572_235-3571delinsTG ENSP00000260943.7:n.235-3572_235-3571delinsTG
ENST00000342788.9:c.235-3572_235-3571delinsTG MANE Select ENSP00000342235.4:n.235-3572_235-3571delinsTG
ENST00000402597.6:c.157-3572_157-3571delinsTG ENSP00000385565.3:n.157-3572_157-3571delinsTG
ENST00000260943.10:c.234-3572_234-3571delinsTG
ENST00000342788.8:c.235-3572_235-3571delinsTG ENSP00000342235.4:n.235-3572_235-3571delinsTG
ENST00000402597.5:c.58-3572_58-3571delinsTG ENSP00000385565.2:n.58-3572_58-3571delinsTG
ENST00000435846.1:c.58-3572_58-3571delinsTG ENSP00000405564.1:n.58-3572_58-3571delinsTG
ENST00000436443.5:c.235-3572_235-3571delinsTG ENSP00000403204.1:n.235-3572_235-3571delinsTG
ENST00000484474.1:n.152-3572_152-3571delinsTG
ENST00000484594.5:n.287-3572_287-3571delinsTG
NM_001042599.1:c.235-3572_235-3571delinsTG NP_001036064.1:n.235-3572_235-3571delinsTG
NM_005235.2:c.235-3572_235-3571delinsTG NP_005226.1:n.235-3572_235-3571delinsTG
XM_005246375.1:c.235-3572_235-3571delinsTG XP_005246432.1:n.235-3572_235-3571delinsTG
XM_005246376.1:c.235-3572_235-3571delinsTG XP_005246433.1:n.235-3572_235-3571delinsTG
XM_005246377.1:c.235-3572_235-3571delinsTG XP_005246434.1:n.235-3572_235-3571delinsTG
XM_006712364.1:c.235-3572_235-3571delinsTG XP_006712427.1:n.235-3572_235-3571delinsTG
XM_005246376.3:c.235-3572_235-3571delinsTG XP_005246433.1:n.235-3572_235-3571delinsTG
XM_005246377.3:c.235-3572_235-3571delinsTG XP_005246434.1:n.235-3572_235-3571delinsTG
XM_006712364.3:c.235-3572_235-3571delinsTG XP_006712427.1:n.235-3572_235-3571delinsTG
XM_017003577.2:c.235-3572_235-3571delinsTG XP_016859066.1:n.235-3572_235-3571delinsTG
XM_017003578.2:c.235-3572_235-3571delinsTG XP_016859067.1:n.235-3572_235-3571delinsTG
XM_017003579.2:c.235-3572_235-3571delinsTG XP_016859068.1:n.235-3572_235-3571delinsTG
XM_017003580.2:c.235-3572_235-3571delinsTG XP_016859069.1:n.235-3572_235-3571delinsTG
XM_017003581.2:c.235-3572_235-3571delinsTG XP_016859070.1:n.235-3572_235-3571delinsTG
NM_005235.3:c.235-3572_235-3571delinsTG MANE Select NP_005226.1:n.235-3572_235-3571delinsTG