Canonical Allele Identifier: CA65137672

Gene: ERBB4

Linked Data

• dbSNP Id: rs769728598
• gnomAD v3: 2-211377040-A-AAT
• gnomAD v4: 2-211377040-A-AAT
• MyVariant Identifiers: chr2:g.212241765_212241766insAT (hg19) ; chr2:g.211377040_211377041insAT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.211377042_211377043dup , CM000664.2:g.211377042_211377043dup	GRCh38
NC_000002.11:g.212241767_212241768dup , CM000664.1:g.212241767_212241768dup	GRCh37
NC_000002.10:g.211950012_211950013dup	NCBI36
NG_011805.1:g.1166586_1166587dup
NG_011805.2:g.1166587_1166588dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342788.9:c.*6573_*6574dup MANE Select	ENSP00000342235.4:n.*6573_*6574dup
ENST00000402597.6:c.10374_10375dup	ENSP00000385565.3:n.10374_10375dup
ENST00000342788.8:c.*6573_*6574dup	ENSP00000342235.4:n.*6573_*6574dup
ENST00000402597.5:c.*6573_*6574dup	ENSP00000385565.2:n.*6573_*6574dup
ENST00000436443.5:c.*6573_*6574dup	ENSP00000403204.1:n.*6573_*6574dup
NM_001042599.1:c.*6573_*6574dup	NP_001036064.1:n.*6573_*6574dup
NM_005235.2:c.*6573_*6574dup	NP_005226.1:n.*6573_*6574dup
XM_005246375.1:c.*6573_*6574dup	XP_005246432.1:n.*6573_*6574dup
XM_005246376.1:c.*6573_*6574dup	XP_005246433.1:n.*6573_*6574dup
XM_005246377.1:c.*6573_*6574dup	XP_005246434.1:n.*6573_*6574dup
XM_006712364.1:c.*6573_*6574dup	XP_006712427.1:n.*6573_*6574dup
XM_005246376.3:c.*6573_*6574dup	XP_005246433.1:n.*6573_*6574dup
XM_005246377.3:c.*6573_*6574dup	XP_005246434.1:n.*6573_*6574dup
XM_006712364.3:c.*6573_*6574dup	XP_006712427.1:n.*6573_*6574dup
XM_017003577.2:c.*6573_*6574dup	XP_016859066.1:n.*6573_*6574dup
XM_017003578.2:c.*6573_*6574dup	XP_016859067.1:n.*6573_*6574dup
XM_017003579.2:c.*6573_*6574dup	XP_016859068.1:n.*6573_*6574dup
XM_017003580.2:c.*6573_*6574dup	XP_016859069.1:n.*6573_*6574dup
XM_017003581.2:c.*6573_*6574dup	XP_016859070.1:n.*6573_*6574dup
XM_017003582.1:c.*6573_*6574dup	XP_016859071.1:n.*6573_*6574dup
NM_005235.3:c.*6573_*6574dup MANE Select	NP_005226.1:n.*6573_*6574dup