Canonical Allele Identifier: CA1325459810
Gene: ERBB4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.211377036A= , CM000664.2:g.211377036A= GRCh38
NC_000002.11:g.212241761A= , CM000664.1:g.212241761A= GRCh37
NC_000002.10:g.211950006A= NCBI36
NG_011805.1:g.1166592T=
NG_011805.2:g.1166593T=

Transcript Alleles

HGVS Amino-acid change
ENST00000342788.9:c.*6579T= MANE Select ENSP00000342235.4:n.*6579T=
ENST00000402597.6:c.10380T= ENSP00000385565.3:n.10380T=
ENST00000342788.8:c.*6579T= ENSP00000342235.4:n.*6579T=
ENST00000402597.5:c.*6579T= ENSP00000385565.2:n.*6579T=
ENST00000436443.5:c.*6579T= ENSP00000403204.1:n.*6579T=
NM_001042599.1:c.*6579T= NP_001036064.1:n.*6579T=
NM_005235.2:c.*6579T= NP_005226.1:n.*6579T=
XM_005246375.1:c.*6579T= XP_005246432.1:n.*6579T=
XM_005246376.1:c.*6579T= XP_005246433.1:n.*6579T=
XM_005246377.1:c.*6579T= XP_005246434.1:n.*6579T=
XM_006712364.1:c.*6579T= XP_006712427.1:n.*6579T=
XM_005246376.3:c.*6579T= XP_005246433.1:n.*6579T=
XM_005246377.3:c.*6579T= XP_005246434.1:n.*6579T=
XM_006712364.3:c.*6579T= XP_006712427.1:n.*6579T=
XM_017003577.2:c.*6579T= XP_016859066.1:n.*6579T=
XM_017003578.2:c.*6579T= XP_016859067.1:n.*6579T=
XM_017003579.2:c.*6579T= XP_016859068.1:n.*6579T=
XM_017003580.2:c.*6579T= XP_016859069.1:n.*6579T=
XM_017003581.2:c.*6579T= XP_016859070.1:n.*6579T=
XM_017003582.1:c.*6579T= XP_016859071.1:n.*6579T=
NM_005235.3:c.*6579T= MANE Select NP_005226.1:n.*6579T=