Canonical Allele Identifier: CA2087444

Gene: ERBB4

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.211386901G>T , CM000664.2:g.211386901G>T	GRCh38
NC_000002.11:g.212251626G>T , CM000664.1:g.212251626G>T	GRCh37
NC_000002.10:g.211959871G>T	NCBI36
NG_011805.1:g.1156727C>A
NG_011805.2:g.1156728C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_005235.3:c.3433C>A MANE Select	NP_005226.1:p.Leu1145Met
ENST00000342788.9:c.3433C>A MANE Select	ENSP00000342235.4:p.Leu1145Met
NM_001042599.1:c.3385C>A	NP_001036064.1:p.Leu1129Met
NM_005235.2:c.3433C>A	NP_005226.1:p.Leu1145Met
ENST00000260943.11:c.3355C>A	ENSP00000260943.7:p.Leu1119Met
ENST00000342788.8:c.3433C>A	ENSP00000342235.4:p.Leu1145Met
ENST00000402597.5:c.3256C>A	ENSP00000385565.2:p.Leu1086Met
ENST00000402597.6:c.3307C>A	ENSP00000385565.3:p.Leu1103Met
ENST00000436443.5:c.3385C>A	ENSP00000403204.1:p.Leu1129Met
XM_005246375.1:c.3430C>A	XP_005246432.1:p.Leu1144Met
XM_005246376.1:c.3403C>A	XP_005246433.1:p.Leu1135Met
XM_005246376.3:c.3403C>A	XP_005246433.1:p.Leu1135Met
XM_005246377.1:c.3355C>A	XP_005246434.1:p.Leu1119Met
XM_005246377.3:c.3355C>A	XP_005246434.1:p.Leu1119Met
XM_006712364.1:c.3478C>A	XP_006712427.1:p.Leu1160Met
XM_006712364.3:c.3478C>A	XP_006712427.1:p.Leu1160Met
XM_017003577.2:c.3556C>A	XP_016859066.1:p.Leu1186Met
XM_017003578.2:c.3511C>A	XP_016859067.1:p.Leu1171Met
XM_017003579.2:c.3508C>A	XP_016859068.1:p.Leu1170Met
XM_017003580.2:c.3481C>A	XP_016859069.1:p.Leu1161Met
XM_017003581.2:c.3463C>A	XP_016859070.1:p.Leu1155Met
XM_017003582.1:c.2857C>A	XP_016859071.1:p.Leu953Met