Canonical Allele Identifier: CA11136762

Gene: ERBB4

Linked Data

• dbSNP Id: rs16845990
• gnomAD v2: 2-212243011-T-C
• gnomAD v3: 2-211378286-T-C
• gnomAD v4: 2-211378286-T-C
• MyVariant Identifiers: chr2:g.212243011T>C (hg19) ; chr2:g.211378286T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.211378286T>C , CM000664.2:g.211378286T>C	GRCh38
NC_000002.11:g.212243011T>C , CM000664.1:g.212243011T>C	GRCh37
NC_000002.10:g.211951256T>C	NCBI36
NG_011805.1:g.1165342A>G
NG_011805.2:g.1165343A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000342788.9:c.*5329A>G MANE Select	ENSP00000342235.4:n.*5329A>G
ENST00000402597.6:c.9130A>G	ENSP00000385565.3:n.9130A>G
ENST00000342788.8:c.*5329A>G	ENSP00000342235.4:n.*5329A>G
ENST00000402597.5:c.*5329A>G	ENSP00000385565.2:n.*5329A>G
ENST00000436443.5:c.*5329A>G	ENSP00000403204.1:n.*5329A>G
NM_001042599.1:c.*5329A>G	NP_001036064.1:n.*5329A>G
NM_005235.2:c.*5329A>G	NP_005226.1:n.*5329A>G
XM_005246375.1:c.*5329A>G	XP_005246432.1:n.*5329A>G
XM_005246376.1:c.*5329A>G	XP_005246433.1:n.*5329A>G
XM_005246377.1:c.*5329A>G	XP_005246434.1:n.*5329A>G
XM_006712364.1:c.*5329A>G	XP_006712427.1:n.*5329A>G
XM_005246376.3:c.*5329A>G	XP_005246433.1:n.*5329A>G
XM_005246377.3:c.*5329A>G	XP_005246434.1:n.*5329A>G
XM_006712364.3:c.*5329A>G	XP_006712427.1:n.*5329A>G
XM_017003577.2:c.*5329A>G	XP_016859066.1:n.*5329A>G
XM_017003578.2:c.*5329A>G	XP_016859067.1:n.*5329A>G
XM_017003579.2:c.*5329A>G	XP_016859068.1:n.*5329A>G
XM_017003580.2:c.*5329A>G	XP_016859069.1:n.*5329A>G
XM_017003581.2:c.*5329A>G	XP_016859070.1:n.*5329A>G
XM_017003582.1:c.*5329A>G	XP_016859071.1:n.*5329A>G
NM_005235.3:c.*5329A>G MANE Select	NP_005226.1:n.*5329A>G