Canonical Allele Identifier: CA2088369

Gene: ERBB4

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.211725192T>A , CM000664.2:g.211725192T>A	GRCh38
NC_000002.11:g.212589917T>A , CM000664.1:g.212589917T>A	GRCh37
NC_000002.10:g.212298162T>A	NCBI36
NG_011805.1:g.818436A>T
NG_011805.2:g.818437A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_005235.3:c.625A>T MANE Select	NP_005226.1:p.Thr209Ser
ENST00000342788.9:c.625A>T MANE Select	ENSP00000342235.4:p.Thr209Ser
NM_001042599.1:c.625A>T	NP_001036064.1:p.Thr209Ser
NM_005235.2:c.625A>T	NP_005226.1:p.Thr209Ser
ENST00000260943.10:c.624A>T
ENST00000260943.11:c.625A>T	ENSP00000260943.7:p.Thr209Ser
ENST00000342788.8:c.625A>T	ENSP00000342235.4:p.Thr209Ser
ENST00000402597.5:c.448A>T	ENSP00000385565.2:p.Thr150Ser
ENST00000402597.6:c.547A>T	ENSP00000385565.3:p.Thr183Ser
ENST00000436443.5:c.625A>T	ENSP00000403204.1:p.Thr209Ser
ENST00000484474.1:n.542A>T
ENST00000484594.5:n.677A>T
XM_005246375.1:c.625A>T	XP_005246432.1:p.Thr209Ser
XM_005246376.1:c.625A>T	XP_005246433.1:p.Thr209Ser
XM_005246376.3:c.625A>T	XP_005246433.1:p.Thr209Ser
XM_005246377.1:c.625A>T	XP_005246434.1:p.Thr209Ser
XM_005246377.3:c.625A>T	XP_005246434.1:p.Thr209Ser
XM_006712364.1:c.625A>T	XP_006712427.1:p.Thr209Ser
XM_006712364.3:c.625A>T	XP_006712427.1:p.Thr209Ser
XM_017003577.2:c.703A>T	XP_016859066.1:p.Thr235Ser
XM_017003578.2:c.703A>T	XP_016859067.1:p.Thr235Ser
XM_017003579.2:c.703A>T	XP_016859068.1:p.Thr235Ser
XM_017003580.2:c.703A>T	XP_016859069.1:p.Thr235Ser
XM_017003581.2:c.703A>T	XP_016859070.1:p.Thr235Ser
XM_017003582.1:c.4A>T	XP_016859071.1:p.Thr2Ser