Canonical Allele Identifier: CA350442408

Gene: ERBB4

Linked Data

• MyVariant Identifiers: chr2:g.212566801A>C (hg19) ; chr2:g.211702076A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.211702076A>C , CM000664.2:g.211702076A>C	GRCh38
NC_000002.11:g.212566801A>C , CM000664.1:g.212566801A>C	GRCh37
NC_000002.10:g.212275046A>C	NCBI36
NG_011805.1:g.841552T>G
NG_011805.2:g.841553T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260943.11:c.1380T>G	ENSP00000260943.7:p.Ile460Met
ENST00000342788.9:c.1380T>G MANE Select	ENSP00000342235.4:p.Ile460Met
ENST00000402597.6:c.1302T>G	ENSP00000385565.3:p.Ile434Met
ENST00000260943.10:c.1379T>G
ENST00000342788.8:c.1380T>G	ENSP00000342235.4:p.Ile460Met
ENST00000402597.5:c.1203T>G	ENSP00000385565.2:p.Ile401Met
ENST00000436443.5:c.1380T>G	ENSP00000403204.1:p.Ile460Met
ENST00000484594.5:n.1432T>G
NM_001042599.1:c.1380T>G	NP_001036064.1:p.Ile460Met
NM_005235.2:c.1380T>G	NP_005226.1:p.Ile460Met
XM_005246375.1:c.1380T>G	XP_005246432.1:p.Ile460Met
XM_005246376.1:c.1380T>G	XP_005246433.1:p.Ile460Met
XM_005246377.1:c.1380T>G	XP_005246434.1:p.Ile460Met
XM_006712364.1:c.1380T>G	XP_006712427.1:p.Ile460Met
XM_005246376.3:c.1380T>G	XP_005246433.1:p.Ile460Met
XM_005246377.3:c.1380T>G	XP_005246434.1:p.Ile460Met
XM_006712364.3:c.1380T>G	XP_006712427.1:p.Ile460Met
XM_017003577.2:c.1458T>G	XP_016859066.1:p.Ile486Met
XM_017003578.2:c.1458T>G	XP_016859067.1:p.Ile486Met
XM_017003579.2:c.1458T>G	XP_016859068.1:p.Ile486Met
XM_017003580.2:c.1458T>G	XP_016859069.1:p.Ile486Met
XM_017003581.2:c.1458T>G	XP_016859070.1:p.Ile486Met
XM_017003582.1:c.759T>G	XP_016859071.1:p.Ile253Met
NM_005235.3:c.1380T>G MANE Select	NP_005226.1:p.Ile460Met