Canonical Allele Identifier: CA2662941693

Gene: ERBB4

Linked Data

• gnomAD v4: 2-211377829-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.211377829A>G , CM000664.2:g.211377829A>G	GRCh38
NC_000002.11:g.212242554A>G , CM000664.1:g.212242554A>G	GRCh37
NC_000002.10:g.211950799A>G	NCBI36
NG_011805.1:g.1165799T>C
NG_011805.2:g.1165800T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000342788.9:c.*5786T>C MANE Select	ENSP00000342235.4:n.*5786T>C
ENST00000402597.6:c.9587T>C	ENSP00000385565.3:n.9587T>C
ENST00000342788.8:c.*5786T>C	ENSP00000342235.4:n.*5786T>C
ENST00000402597.5:c.*5786T>C	ENSP00000385565.2:n.*5786T>C
ENST00000436443.5:c.*5786T>C	ENSP00000403204.1:n.*5786T>C
NM_001042599.1:c.*5786T>C	NP_001036064.1:n.*5786T>C
NM_005235.2:c.*5786T>C	NP_005226.1:n.*5786T>C
XM_005246375.1:c.*5786T>C	XP_005246432.1:n.*5786T>C
XM_005246376.1:c.*5786T>C	XP_005246433.1:n.*5786T>C
XM_005246377.1:c.*5786T>C	XP_005246434.1:n.*5786T>C
XM_006712364.1:c.*5786T>C	XP_006712427.1:n.*5786T>C
XM_005246376.3:c.*5786T>C	XP_005246433.1:n.*5786T>C
XM_005246377.3:c.*5786T>C	XP_005246434.1:n.*5786T>C
XM_006712364.3:c.*5786T>C	XP_006712427.1:n.*5786T>C
XM_017003577.2:c.*5786T>C	XP_016859066.1:n.*5786T>C
XM_017003578.2:c.*5786T>C	XP_016859067.1:n.*5786T>C
XM_017003579.2:c.*5786T>C	XP_016859068.1:n.*5786T>C
XM_017003580.2:c.*5786T>C	XP_016859069.1:n.*5786T>C
XM_017003581.2:c.*5786T>C	XP_016859070.1:n.*5786T>C
XM_017003582.1:c.*5786T>C	XP_016859071.1:n.*5786T>C
NM_005235.3:c.*5786T>C MANE Select	NP_005226.1:n.*5786T>C