Canonical Allele Identifier: CA1325785575

Gene: ERBB4

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.212050001C>G , CM000664.2:g.212050001C>G	GRCh38
NC_000002.11:g.212914726C>G , CM000664.1:g.212914726C>G	GRCh37
NC_000002.10:g.212622971C>G	NCBI36
NG_011805.1:g.493627G>C
NG_011805.2:g.493628G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260943.11:c.234+74751G>C	ENSP00000260943.7:n.234+74751G>C
ENST00000342788.9:c.234+74751G>C MANE Select	ENSP00000342235.4:n.234+74751G>C
ENST00000402597.6:c.156+74751G>C	ENSP00000385565.3:n.156+74751G>C
ENST00000260943.10:c.233+74751G>C
ENST00000342788.8:c.234+74751G>C	ENSP00000342235.4:n.234+74751G>C
ENST00000402597.5:c.57+74751G>C	ENSP00000385565.2:n.57+74751G>C
ENST00000435846.1:c.57+74751G>C	ENSP00000405564.1:n.57+74751G>C
ENST00000436443.5:c.234+74751G>C	ENSP00000403204.1:n.234+74751G>C
ENST00000484594.5:n.286+74751G>C
NM_001042599.1:c.234+74751G>C	NP_001036064.1:n.234+74751G>C
NM_005235.2:c.234+74751G>C	NP_005226.1:n.234+74751G>C
XM_005246375.1:c.234+74751G>C	XP_005246432.1:n.234+74751G>C
XM_005246376.1:c.234+74751G>C	XP_005246433.1:n.234+74751G>C
XM_005246377.1:c.234+74751G>C	XP_005246434.1:n.234+74751G>C
XM_006712364.1:c.234+74751G>C	XP_006712427.1:n.234+74751G>C
XM_005246376.3:c.234+74751G>C	XP_005246433.1:n.234+74751G>C
XM_005246377.3:c.234+74751G>C	XP_005246434.1:n.234+74751G>C
XM_006712364.3:c.234+74751G>C	XP_006712427.1:n.234+74751G>C
XM_017003577.2:c.234+74751G>C	XP_016859066.1:n.234+74751G>C
XM_017003578.2:c.234+74751G>C	XP_016859067.1:n.234+74751G>C
XM_017003579.2:c.234+74751G>C	XP_016859068.1:n.234+74751G>C
XM_017003580.2:c.234+74751G>C	XP_016859069.1:n.234+74751G>C
XM_017003581.2:c.234+74751G>C	XP_016859070.1:n.234+74751G>C
NM_005235.3:c.234+74751G>C MANE Select	NP_005226.1:n.234+74751G>C