Canonical Allele Identifier: CA350442327

Gene: ERBB4

Linked Data

• MyVariant Identifiers: chr2:g.212566767T>A (hg19) ; chr2:g.211702042T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.211702042T>A , CM000664.2:g.211702042T>A	GRCh38
NC_000002.11:g.212566767T>A , CM000664.1:g.212566767T>A	GRCh37
NC_000002.10:g.212275012T>A	NCBI36
NG_011805.1:g.841586A>T
NG_011805.2:g.841587A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260943.11:c.1414A>T	ENSP00000260943.7:p.Ile472Phe
ENST00000342788.9:c.1414A>T MANE Select	ENSP00000342235.4:p.Ile472Phe
ENST00000402597.6:c.1336A>T	ENSP00000385565.3:p.Ile446Phe
ENST00000260943.10:c.1413A>T
ENST00000342788.8:c.1414A>T	ENSP00000342235.4:p.Ile472Phe
ENST00000402597.5:c.1237A>T	ENSP00000385565.2:p.Ile413Phe
ENST00000436443.5:c.1414A>T	ENSP00000403204.1:p.Ile472Phe
ENST00000484594.5:n.1466A>T
NM_001042599.1:c.1414A>T	NP_001036064.1:p.Ile472Phe
NM_005235.2:c.1414A>T	NP_005226.1:p.Ile472Phe
XM_005246375.1:c.1414A>T	XP_005246432.1:p.Ile472Phe
XM_005246376.1:c.1414A>T	XP_005246433.1:p.Ile472Phe
XM_005246377.1:c.1414A>T	XP_005246434.1:p.Ile472Phe
XM_006712364.1:c.1414A>T	XP_006712427.1:p.Ile472Phe
XM_005246376.3:c.1414A>T	XP_005246433.1:p.Ile472Phe
XM_005246377.3:c.1414A>T	XP_005246434.1:p.Ile472Phe
XM_006712364.3:c.1414A>T	XP_006712427.1:p.Ile472Phe
XM_017003577.2:c.1492A>T	XP_016859066.1:p.Ile498Phe
XM_017003578.2:c.1492A>T	XP_016859067.1:p.Ile498Phe
XM_017003579.2:c.1492A>T	XP_016859068.1:p.Ile498Phe
XM_017003580.2:c.1492A>T	XP_016859069.1:p.Ile498Phe
XM_017003581.2:c.1492A>T	XP_016859070.1:p.Ile498Phe
XM_017003582.1:c.793A>T	XP_016859071.1:p.Ile265Phe
NM_005235.3:c.1414A>T MANE Select	NP_005226.1:p.Ile472Phe