Canonical Allele Identifier: CA1325460170
Gene: ERBB4 HGNC NCBI

Linked Data

dbSNP Id: rs2062501783

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.211377817_211377820dup , CM000664.2:g.211377817_211377820dup GRCh38
NC_000002.11:g.212242542_212242545dup , CM000664.1:g.212242542_212242545dup GRCh37
NC_000002.10:g.211950787_211950790dup NCBI36
NG_011805.1:g.1165808_1165811dup
NG_011805.2:g.1165809_1165812dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000342788.9:c.*5795_*5798dup MANE Select ENSP00000342235.4:n.*5795_*5798dup
ENST00000402597.6:c.9596_9599dup ENSP00000385565.3:n.9596_9599dup
ENST00000342788.8:c.*5795_*5798dup ENSP00000342235.4:n.*5795_*5798dup
ENST00000402597.5:c.*5795_*5798dup ENSP00000385565.2:n.*5795_*5798dup
ENST00000436443.5:c.*5795_*5798dup ENSP00000403204.1:n.*5795_*5798dup
NM_001042599.1:c.*5795_*5798dup NP_001036064.1:n.*5795_*5798dup
NM_005235.2:c.*5795_*5798dup NP_005226.1:n.*5795_*5798dup
XM_005246375.1:c.*5795_*5798dup XP_005246432.1:n.*5795_*5798dup
XM_005246376.1:c.*5795_*5798dup XP_005246433.1:n.*5795_*5798dup
XM_005246377.1:c.*5795_*5798dup XP_005246434.1:n.*5795_*5798dup
XM_006712364.1:c.*5795_*5798dup XP_006712427.1:n.*5795_*5798dup
XM_005246376.3:c.*5795_*5798dup XP_005246433.1:n.*5795_*5798dup
XM_005246377.3:c.*5795_*5798dup XP_005246434.1:n.*5795_*5798dup
XM_006712364.3:c.*5795_*5798dup XP_006712427.1:n.*5795_*5798dup
XM_017003577.2:c.*5795_*5798dup XP_016859066.1:n.*5795_*5798dup
XM_017003578.2:c.*5795_*5798dup XP_016859067.1:n.*5795_*5798dup
XM_017003579.2:c.*5795_*5798dup XP_016859068.1:n.*5795_*5798dup
XM_017003580.2:c.*5795_*5798dup XP_016859069.1:n.*5795_*5798dup
XM_017003581.2:c.*5795_*5798dup XP_016859070.1:n.*5795_*5798dup
XM_017003582.1:c.*5795_*5798dup XP_016859071.1:n.*5795_*5798dup
NM_005235.3:c.*5795_*5798dup MANE Select NP_005226.1:n.*5795_*5798dup