Canonical Allele Identifier: CA2088156

Gene: ERBB4

Linked Data

• dbSNP Id: rs765657644
• ExAC: 2:212566895 A / T
• gnomAD v2: 2-212566895-A-T
• gnomAD v4: 2-211702170-A-T
• MyVariant Identifiers: chr2:g.212566895A>T (hg19) ; chr2:g.211702170A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.211702170A>T , CM000664.2:g.211702170A>T	GRCh38
NC_000002.11:g.212566895A>T , CM000664.1:g.212566895A>T	GRCh37
NC_000002.10:g.212275140A>T	NCBI36
NG_011805.1:g.841458T>A
NG_011805.2:g.841459T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260943.11:c.1290-4T>A	ENSP00000260943.7:n.1290-4T>A
ENST00000342788.9:c.1290-4T>A MANE Select	ENSP00000342235.4:n.1290-4T>A
ENST00000402597.6:c.1212-4T>A	ENSP00000385565.3:n.1212-4T>A
ENST00000260943.10:c.1289-4T>A
ENST00000342788.8:c.1290-4T>A	ENSP00000342235.4:n.1290-4T>A
ENST00000402597.5:c.1113-4T>A	ENSP00000385565.2:n.1113-4T>A
ENST00000436443.5:c.1290-4T>A	ENSP00000403204.1:n.1290-4T>A
ENST00000484594.5:n.1342-4T>A
NM_001042599.1:c.1290-4T>A	NP_001036064.1:n.1290-4T>A
NM_005235.2:c.1290-4T>A	NP_005226.1:n.1290-4T>A
XM_005246375.1:c.1290-4T>A	XP_005246432.1:n.1290-4T>A
XM_005246376.1:c.1290-4T>A	XP_005246433.1:n.1290-4T>A
XM_005246377.1:c.1290-4T>A	XP_005246434.1:n.1290-4T>A
XM_006712364.1:c.1290-4T>A	XP_006712427.1:n.1290-4T>A
XM_005246376.3:c.1290-4T>A	XP_005246433.1:n.1290-4T>A
XM_005246377.3:c.1290-4T>A	XP_005246434.1:n.1290-4T>A
XM_006712364.3:c.1290-4T>A	XP_006712427.1:n.1290-4T>A
XM_017003577.2:c.1368-4T>A	XP_016859066.1:n.1368-4T>A
XM_017003578.2:c.1368-4T>A	XP_016859067.1:n.1368-4T>A
XM_017003579.2:c.1368-4T>A	XP_016859068.1:n.1368-4T>A
XM_017003580.2:c.1368-4T>A	XP_016859069.1:n.1368-4T>A
XM_017003581.2:c.1368-4T>A	XP_016859070.1:n.1368-4T>A
XM_017003582.1:c.669-4T>A	XP_016859071.1:n.669-4T>A
NM_005235.3:c.1290-4T>A MANE Select	NP_005226.1:n.1290-4T>A