Canonical Allele Identifier: CA350442607
Gene: ERBB4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.211702166A>T , CM000664.2:g.211702166A>T GRCh38
NC_000002.11:g.212566891A>T , CM000664.1:g.212566891A>T GRCh37
NC_000002.10:g.212275136A>T NCBI36
NG_011805.1:g.841462T>A
NG_011805.2:g.841463T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000260943.11:c.1290T>A ENSP00000260943.7:p.Ser430Arg
ENST00000342788.9:c.1290T>A MANE Select ENSP00000342235.4:p.Ser430Arg
ENST00000402597.6:c.1212T>A ENSP00000385565.3:p.Ser404Arg
ENST00000260943.10:c.1289T>A
ENST00000342788.8:c.1290T>A ENSP00000342235.4:p.Ser430Arg
ENST00000402597.5:c.1113T>A ENSP00000385565.2:p.Ser371Arg
ENST00000436443.5:c.1290T>A ENSP00000403204.1:p.Ser430Arg
ENST00000484594.5:n.1342T>A
NM_001042599.1:c.1290T>A NP_001036064.1:p.Ser430Arg
NM_005235.2:c.1290T>A NP_005226.1:p.Ser430Arg
XM_005246375.1:c.1290T>A XP_005246432.1:p.Ser430Arg
XM_005246376.1:c.1290T>A XP_005246433.1:p.Ser430Arg
XM_005246377.1:c.1290T>A XP_005246434.1:p.Ser430Arg
XM_006712364.1:c.1290T>A XP_006712427.1:p.Ser430Arg
XM_005246376.3:c.1290T>A XP_005246433.1:p.Ser430Arg
XM_005246377.3:c.1290T>A XP_005246434.1:p.Ser430Arg
XM_006712364.3:c.1290T>A XP_006712427.1:p.Ser430Arg
XM_017003577.2:c.1368T>A XP_016859066.1:p.Ser456Arg
XM_017003578.2:c.1368T>A XP_016859067.1:p.Ser456Arg
XM_017003579.2:c.1368T>A XP_016859068.1:p.Ser456Arg
XM_017003580.2:c.1368T>A XP_016859069.1:p.Ser456Arg
XM_017003581.2:c.1368T>A XP_016859070.1:p.Ser456Arg
XM_017003582.1:c.669T>A XP_016859071.1:p.Ser223Arg
NM_005235.3:c.1290T>A MANE Select NP_005226.1:p.Ser430Arg