Canonical Allele Identifier: CA399314316

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37884186C>A (hg19) ; chr17:g.39727933C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727933C>A , CM000679.2:g.39727933C>A	GRCh38
NC_000017.10:g.37884186C>A , CM000679.1:g.37884186C>A	GRCh37
NC_000017.9:g.35137712C>A	NCBI36
NG_007503.1:g.44794C>A , LRG_724:g.44794C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3657C>A MANE Select	ENSP00000269571.4:p.Asn1219Lys
ENST00000269571.9:c.3657C>A	ENSP00000269571.4:p.Asn1219Lys
ENST00000406381.6:c.3567C>A	ENSP00000385185.2:p.Asn1189Lys
ENST00000445658.6:c.2829C>A	ENSP00000404047.2:p.Asn943Lys
ENST00000541774.5:c.3612C>A	ENSP00000446466.1:p.Asn1204Lys
ENST00000578373.5:c.*3447C>A	ENSP00000463427.1:n.*3447C>A
ENST00000584450.5:c.*236C>A	ENSP00000463714.1:n.*236C>A
ENST00000584601.5:c.3567C>A	ENSP00000462438.1:p.Asn1189Lys
NM_001005862.2:c.3567C>A , LRG_724t1:c.3567C>A	NP_001005862.1:p.Asn1189Lys
NM_001289936.1:c.3612C>A , LRG_724t4:c.3612C>A	NP_001276865.1:p.Asn1204Lys
NM_001289937.1:c.*236C>A	NP_001276866.1:n.*236C>A
NM_004448.3:c.3657C>A , LRG_724t2:c.3657C>A	NP_004439.2:p.Asn1219Lys
NR_110535.1:n.3981C>A
XM_024450641.1:c.3795C>A	XP_024306409.1:p.Asn1265Lys
XM_024450642.1:c.3750C>A	XP_024306410.1:p.Asn1250Lys
XM_024450643.1:c.3705C>A	XP_024306411.1:p.Asn1235Lys
NM_001005862.3:c.3567C>A	NP_001005862.1:p.Asn1189Lys
NM_001289936.2:c.3612C>A	NP_001276865.1:p.Asn1204Lys
NM_001289937.2:c.*236C>A	NP_001276866.1:n.*236C>A
NM_001382782.1:c.3567C>A	NP_001369711.1:p.Asn1189Lys
NM_001382783.1:c.3567C>A	NP_001369712.1:p.Asn1189Lys
NM_001382784.1:c.3774C>A	NP_001369713.1:p.Asn1258Lys
NM_001382785.1:c.3759C>A	NP_001369714.1:p.Asn1253Lys
NM_001382786.1:c.3738C>A	NP_001369715.1:p.Asn1246Lys
NM_001382787.1:c.3732C>A	NP_001369716.1:p.Asn1244Lys
NM_001382788.1:c.3687C>A	NP_001369717.1:p.Asn1229Lys
NM_001382789.1:c.3678C>A	NP_001369718.1:p.Asn1226Lys
NM_001382790.1:c.3654C>A	NP_001369719.1:p.Asn1218Lys
NM_001382791.1:c.3648C>A	NP_001369720.1:p.Asn1216Lys
NM_001382792.1:c.3621C>A	NP_001369721.1:p.Asn1207Lys
NM_001382793.1:c.3615C>A	NP_001369722.1:p.Asn1205Lys
NM_001382794.1:c.3615C>A	NP_001369723.1:p.Asn1205Lys
NM_001382795.1:c.3609C>A	NP_001369724.1:p.Asn1203Lys
NM_001382796.1:c.3570C>A	NP_001369725.1:p.Asn1190Lys
NM_001382797.1:c.3558C>A	NP_001369726.1:p.Asn1186Lys
NM_001382798.1:c.3501C>A	NP_001369727.1:p.Asn1167Lys
NM_001382799.1:c.3477C>A	NP_001369728.1:p.Asn1159Lys
NM_001382800.1:c.3471C>A	NP_001369729.1:p.Asn1157Lys
NM_001382801.1:c.3453C>A	NP_001369730.1:p.Asn1151Lys
NM_001382802.1:c.3399C>A	NP_001369731.1:p.Asn1133Lys
NM_001382803.1:c.*236C>A	NP_001369732.1:n.*236C>A
NM_001382804.1:c.2829C>A	NP_001369733.1:p.Asn943Lys
NM_001382805.1:c.2706C>A	NP_001369734.1:p.Asn902Lys
NM_001382806.1:c.2619C>A	NP_001369735.1:p.Asn873Lys
NM_004448.4:c.3657C>A MANE Select	NP_004439.2:p.Asn1219Lys
NR_110535.2:n.3895C>A