Canonical Allele Identifier: CA350443725

Gene: ERBB4

Linked Data

• dbSNP Id: rs267599193
• MyVariant Identifiers: chr2:g.212578308C>A (hg19) ; chr2:g.211713583C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.211713583C>A , CM000664.2:g.211713583C>A	GRCh38
NC_000002.11:g.212578308C>A , CM000664.1:g.212578308C>A	GRCh37
NC_000002.10:g.212286553C>A	NCBI36
NG_011805.1:g.830045G>T
NG_011805.2:g.830046G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000260943.11:c.949G>T	ENSP00000260943.7:p.Glu317Ter
ENST00000342788.9:c.949G>T MANE Select	ENSP00000342235.4:p.Glu317Ter
ENST00000402597.6:c.871G>T	ENSP00000385565.3:p.Glu291Ter
ENST00000260943.10:c.948G>T
ENST00000342788.8:c.949G>T	ENSP00000342235.4:p.Glu317Ter
ENST00000402597.5:c.772G>T	ENSP00000385565.2:p.Glu258Ter
ENST00000436443.5:c.949G>T	ENSP00000403204.1:p.Glu317Ter
ENST00000484594.5:n.1001G>T
NM_001042599.1:c.949G>T	NP_001036064.1:p.Glu317Ter
NM_005235.2:c.949G>T	NP_005226.1:p.Glu317Ter
XM_005246375.1:c.949G>T	XP_005246432.1:p.Glu317Ter
XM_005246376.1:c.949G>T	XP_005246433.1:p.Glu317Ter
XM_005246377.1:c.949G>T	XP_005246434.1:p.Glu317Ter
XM_006712364.1:c.949G>T	XP_006712427.1:p.Glu317Ter
XM_005246376.3:c.949G>T	XP_005246433.1:p.Glu317Ter
XM_005246377.3:c.949G>T	XP_005246434.1:p.Glu317Ter
XM_006712364.3:c.949G>T	XP_006712427.1:p.Glu317Ter
XM_017003577.2:c.1027G>T	XP_016859066.1:p.Glu343Ter
XM_017003578.2:c.1027G>T	XP_016859067.1:p.Glu343Ter
XM_017003579.2:c.1027G>T	XP_016859068.1:p.Glu343Ter
XM_017003580.2:c.1027G>T	XP_016859069.1:p.Glu343Ter
XM_017003581.2:c.1027G>T	XP_016859070.1:p.Glu343Ter
XM_017003582.1:c.328G>T	XP_016859071.1:p.Glu110Ter
NM_005235.3:c.949G>T MANE Select	NP_005226.1:p.Glu317Ter