Canonical Allele Identifier: CA1325911003
Gene: ERBB4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.212304043G= , CM000664.2:g.212304043G= GRCh38
NC_000002.11:g.213168768G= , CM000664.1:g.213168768G= GRCh37
NC_000002.10:g.212877013G= NCBI36
NG_011805.1:g.239585C=
NG_011805.2:g.239586C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000260943.11:c.83-179140C= ENSP00000260943.7:n.83-179140C=
ENST00000342788.9:c.83-179140C= MANE Select ENSP00000342235.4:n.83-179140C=
ENST00000260943.10:c.82-179140C=
ENST00000342788.8:c.83-179140C= ENSP00000342235.4:n.83-179140C=
ENST00000435846.1:c.-96+125116C= ENSP00000405564.1:n.-96+125116C=
ENST00000436443.5:c.83-179140C= ENSP00000403204.1:n.83-179140C=
ENST00000484594.5:n.135-179140C=
NM_001042599.1:c.83-179140C= NP_001036064.1:n.83-179140C=
NM_005235.2:c.83-179140C= NP_005226.1:n.83-179140C=
XM_005246375.1:c.83-179140C= XP_005246432.1:n.83-179140C=
XM_005246376.1:c.83-179140C= XP_005246433.1:n.83-179140C=
XM_005246377.1:c.83-179140C= XP_005246434.1:n.83-179140C=
XM_006712364.1:c.83-179140C= XP_006712427.1:n.83-179140C=
XM_005246376.3:c.83-179140C= XP_005246433.1:n.83-179140C=
XM_005246377.3:c.83-179140C= XP_005246434.1:n.83-179140C=
XM_006712364.3:c.83-179140C= XP_006712427.1:n.83-179140C=
XM_017003577.2:c.83-179140C= XP_016859066.1:n.83-179140C=
XM_017003578.2:c.83-179140C= XP_016859067.1:n.83-179140C=
XM_017003579.2:c.83-179140C= XP_016859068.1:n.83-179140C=
XM_017003580.2:c.83-179140C= XP_016859069.1:n.83-179140C=
XM_017003581.2:c.83-179140C= XP_016859070.1:n.83-179140C=
NM_005235.3:c.83-179140C= MANE Select NP_005226.1:n.83-179140C=