Canonical Allele Identifier: CA350442491

Gene: ERBB4

Linked Data

• dbSNP Id: rs1466611295
• MyVariant Identifiers: chr2:g.212566838T>G (hg19) ; chr2:g.211702113T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.211702113T>G , CM000664.2:g.211702113T>G	GRCh38
NC_000002.11:g.212566838T>G , CM000664.1:g.212566838T>G	GRCh37
NC_000002.10:g.212275083T>G	NCBI36
NG_011805.1:g.841515A>C
NG_011805.2:g.841516A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000260943.11:c.1343A>C	ENSP00000260943.7:p.Gln448Pro
ENST00000342788.9:c.1343A>C MANE Select	ENSP00000342235.4:p.Gln448Pro
ENST00000402597.6:c.1265A>C	ENSP00000385565.3:p.Gln422Pro
ENST00000260943.10:c.1342A>C
ENST00000342788.8:c.1343A>C	ENSP00000342235.4:p.Gln448Pro
ENST00000402597.5:c.1166A>C	ENSP00000385565.2:p.Gln389Pro
ENST00000436443.5:c.1343A>C	ENSP00000403204.1:p.Gln448Pro
ENST00000484594.5:n.1395A>C
NM_001042599.1:c.1343A>C	NP_001036064.1:p.Gln448Pro
NM_005235.2:c.1343A>C	NP_005226.1:p.Gln448Pro
XM_005246375.1:c.1343A>C	XP_005246432.1:p.Gln448Pro
XM_005246376.1:c.1343A>C	XP_005246433.1:p.Gln448Pro
XM_005246377.1:c.1343A>C	XP_005246434.1:p.Gln448Pro
XM_006712364.1:c.1343A>C	XP_006712427.1:p.Gln448Pro
XM_005246376.3:c.1343A>C	XP_005246433.1:p.Gln448Pro
XM_005246377.3:c.1343A>C	XP_005246434.1:p.Gln448Pro
XM_006712364.3:c.1343A>C	XP_006712427.1:p.Gln448Pro
XM_017003577.2:c.1421A>C	XP_016859066.1:p.Gln474Pro
XM_017003578.2:c.1421A>C	XP_016859067.1:p.Gln474Pro
XM_017003579.2:c.1421A>C	XP_016859068.1:p.Gln474Pro
XM_017003580.2:c.1421A>C	XP_016859069.1:p.Gln474Pro
XM_017003581.2:c.1421A>C	XP_016859070.1:p.Gln474Pro
XM_017003582.1:c.722A>C	XP_016859071.1:p.Gln241Pro
NM_005235.3:c.1343A>C MANE Select	NP_005226.1:p.Gln448Pro