Canonical Allele Identifier: CA350442539

Gene: ERBB4

Linked Data

• dbSNP Id: rs2106037395
• MyVariant Identifiers: chr2:g.212566860C>G (hg19) ; chr2:g.211702135C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.211702135C>G , CM000664.2:g.211702135C>G	GRCh38
NC_000002.11:g.212566860C>G , CM000664.1:g.212566860C>G	GRCh37
NC_000002.10:g.212275105C>G	NCBI36
NG_011805.1:g.841493G>C
NG_011805.2:g.841494G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260943.11:c.1321G>C	ENSP00000260943.7:p.Gly441Arg
ENST00000342788.9:c.1321G>C MANE Select	ENSP00000342235.4:p.Gly441Arg
ENST00000402597.6:c.1243G>C	ENSP00000385565.3:p.Gly415Arg
ENST00000260943.10:c.1320G>C
ENST00000342788.8:c.1321G>C	ENSP00000342235.4:p.Gly441Arg
ENST00000402597.5:c.1144G>C	ENSP00000385565.2:p.Gly382Arg
ENST00000436443.5:c.1321G>C	ENSP00000403204.1:p.Gly441Arg
ENST00000484594.5:n.1373G>C
NM_001042599.1:c.1321G>C	NP_001036064.1:p.Gly441Arg
NM_005235.2:c.1321G>C	NP_005226.1:p.Gly441Arg
XM_005246375.1:c.1321G>C	XP_005246432.1:p.Gly441Arg
XM_005246376.1:c.1321G>C	XP_005246433.1:p.Gly441Arg
XM_005246377.1:c.1321G>C	XP_005246434.1:p.Gly441Arg
XM_006712364.1:c.1321G>C	XP_006712427.1:p.Gly441Arg
XM_005246376.3:c.1321G>C	XP_005246433.1:p.Gly441Arg
XM_005246377.3:c.1321G>C	XP_005246434.1:p.Gly441Arg
XM_006712364.3:c.1321G>C	XP_006712427.1:p.Gly441Arg
XM_017003577.2:c.1399G>C	XP_016859066.1:p.Gly467Arg
XM_017003578.2:c.1399G>C	XP_016859067.1:p.Gly467Arg
XM_017003579.2:c.1399G>C	XP_016859068.1:p.Gly467Arg
XM_017003580.2:c.1399G>C	XP_016859069.1:p.Gly467Arg
XM_017003581.2:c.1399G>C	XP_016859070.1:p.Gly467Arg
XM_017003582.1:c.700G>C	XP_016859071.1:p.Gly234Arg
NM_005235.3:c.1321G>C MANE Select	NP_005226.1:p.Gly441Arg