Canonical Allele Identifier: CA499890858

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37884189C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727936C>A , CM000679.2:g.39727936C>A	GRCh38
NC_000017.10:g.37884189C>A , CM000679.1:g.37884189C>A	GRCh37
NC_000017.9:g.35137715C>A	NCBI36
NG_007503.1:g.44797C>A , LRG_724:g.44797C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3660C>A MANE Select	ENSP00000269571.4:p.Leu1220=
ENST00000269571.9:c.3660C>A	ENSP00000269571.4:p.Leu1220=
ENST00000406381.6:c.3570C>A	ENSP00000385185.2:p.Leu1190=
ENST00000445658.6:c.2832C>A	ENSP00000404047.2:p.Leu944=
ENST00000541774.5:c.3615C>A	ENSP00000446466.1:p.Leu1205=
ENST00000578373.5:c.*3450C>A	ENSP00000463427.1:n.*3450C>A
ENST00000584450.5:c.*239C>A	ENSP00000463714.1:n.*239C>A
ENST00000584601.5:c.3570C>A	ENSP00000462438.1:p.Leu1190=
NM_001005862.2:c.3570C>A , LRG_724t1:c.3570C>A	NP_001005862.1:p.Leu1190=
NM_001289936.1:c.3615C>A , LRG_724t4:c.3615C>A	NP_001276865.1:p.Leu1205=
NM_001289937.1:c.*239C>A	NP_001276866.1:n.*239C>A
NM_004448.3:c.3660C>A , LRG_724t2:c.3660C>A	NP_004439.2:p.Leu1220=
NR_110535.1:n.3984C>A
XM_024450641.1:c.3798C>A	XP_024306409.1:p.Leu1266=
XM_024450642.1:c.3753C>A	XP_024306410.1:p.Leu1251=
XM_024450643.1:c.3708C>A	XP_024306411.1:p.Leu1236=
NM_001005862.3:c.3570C>A	NP_001005862.1:p.Leu1190=
NM_001289936.2:c.3615C>A	NP_001276865.1:p.Leu1205=
NM_001289937.2:c.*239C>A	NP_001276866.1:n.*239C>A
NM_001382782.1:c.3570C>A	NP_001369711.1:p.Leu1190=
NM_001382783.1:c.3570C>A	NP_001369712.1:p.Leu1190=
NM_001382784.1:c.3777C>A	NP_001369713.1:p.Leu1259=
NM_001382785.1:c.3762C>A	NP_001369714.1:p.Leu1254=
NM_001382786.1:c.3741C>A	NP_001369715.1:p.Leu1247=
NM_001382787.1:c.3735C>A	NP_001369716.1:p.Leu1245=
NM_001382788.1:c.3690C>A	NP_001369717.1:p.Leu1230=
NM_001382789.1:c.3681C>A	NP_001369718.1:p.Leu1227=
NM_001382790.1:c.3657C>A	NP_001369719.1:p.Leu1219=
NM_001382791.1:c.3651C>A	NP_001369720.1:p.Leu1217=
NM_001382792.1:c.3624C>A	NP_001369721.1:p.Leu1208=
NM_001382793.1:c.3618C>A	NP_001369722.1:p.Leu1206=
NM_001382794.1:c.3618C>A	NP_001369723.1:p.Leu1206=
NM_001382795.1:c.3612C>A	NP_001369724.1:p.Leu1204=
NM_001382796.1:c.3573C>A	NP_001369725.1:p.Leu1191=
NM_001382797.1:c.3561C>A	NP_001369726.1:p.Leu1187=
NM_001382798.1:c.3504C>A	NP_001369727.1:p.Leu1168=
NM_001382799.1:c.3480C>A	NP_001369728.1:p.Leu1160=
NM_001382800.1:c.3474C>A	NP_001369729.1:p.Leu1158=
NM_001382801.1:c.3456C>A	NP_001369730.1:p.Leu1152=
NM_001382802.1:c.3402C>A	NP_001369731.1:p.Leu1134=
NM_001382803.1:c.*239C>A	NP_001369732.1:n.*239C>A
NM_001382804.1:c.2832C>A	NP_001369733.1:p.Leu944=
NM_001382805.1:c.2709C>A	NP_001369734.1:p.Leu903=
NM_001382806.1:c.2622C>A	NP_001369735.1:p.Leu874=
NM_004448.4:c.3660C>A MANE Select	NP_004439.2:p.Leu1220=
NR_110535.2:n.3898C>A