Canonical Allele Identifier: CA11136894

Gene: ERBB4

Linked Data

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.211928473C>T , CM000664.2:g.211928473C>T	GRCh38
NC_000002.11:g.212793198C>T , CM000664.1:g.212793198C>T	GRCh37
NC_000002.10:g.212501443C>T	NCBI36
NG_011805.1:g.615155G>A
NG_011805.2:g.615156G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260943.11:c.421+18957G>A	ENSP00000260943.7:n.421+18957G>A
ENST00000342788.9:c.421+18957G>A MANE Select	ENSP00000342235.4:n.421+18957G>A
ENST00000402597.6:c.343+18957G>A	ENSP00000385565.3:n.343+18957G>A
ENST00000260943.10:c.420+18957G>A
ENST00000342788.8:c.421+18957G>A	ENSP00000342235.4:n.421+18957G>A
ENST00000402597.5:c.244+18957G>A	ENSP00000385565.2:n.244+18957G>A
ENST00000435846.1:c.244+18957G>A	ENSP00000405564.1:n.244+18957G>A
ENST00000436443.5:c.421+18957G>A	ENSP00000403204.1:n.421+18957G>A
ENST00000484474.1:n.338+18957G>A
ENST00000484594.5:n.473+18957G>A
NM_001042599.1:c.421+18957G>A	NP_001036064.1:n.421+18957G>A
NM_005235.2:c.421+18957G>A	NP_005226.1:n.421+18957G>A
XM_005246375.1:c.421+18957G>A	XP_005246432.1:n.421+18957G>A
XM_005246376.1:c.421+18957G>A	XP_005246433.1:n.421+18957G>A
XM_005246377.1:c.421+18957G>A	XP_005246434.1:n.421+18957G>A
XM_006712364.1:c.421+18957G>A	XP_006712427.1:n.421+18957G>A
XM_005246376.3:c.421+18957G>A	XP_005246433.1:n.421+18957G>A
XM_005246377.3:c.421+18957G>A	XP_005246434.1:n.421+18957G>A
XM_006712364.3:c.421+18957G>A	XP_006712427.1:n.421+18957G>A
XM_017003577.2:c.421+18957G>A	XP_016859066.1:n.421+18957G>A
XM_017003578.2:c.421+18957G>A	XP_016859067.1:n.421+18957G>A
XM_017003579.2:c.421+18957G>A	XP_016859068.1:n.421+18957G>A
XM_017003580.2:c.421+18957G>A	XP_016859069.1:n.421+18957G>A
XM_017003581.2:c.421+18957G>A	XP_016859070.1:n.421+18957G>A
NM_005235.3:c.421+18957G>A MANE Select	NP_005226.1:n.421+18957G>A