Canonical Allele Identifier: CA399313473

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37884075A>T (hg19) ; chr17:g.39727822A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727822A>T , CM000679.2:g.39727822A>T	GRCh38
NC_000017.10:g.37884075A>T , CM000679.1:g.37884075A>T	GRCh37
NC_000017.9:g.35137601A>T	NCBI36
NG_007503.1:g.44683A>T , LRG_724:g.44683A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3546A>T MANE Select	ENSP00000269571.4:p.Lys1182Asn
ENST00000269571.9:c.3546A>T	ENSP00000269571.4:p.Lys1182Asn
ENST00000406381.6:c.3456A>T	ENSP00000385185.2:p.Lys1152Asn
ENST00000445658.6:c.2718A>T	ENSP00000404047.2:p.Lys906Asn
ENST00000541774.5:c.3501A>T	ENSP00000446466.1:p.Lys1167Asn
ENST00000578373.5:c.*3336A>T	ENSP00000463427.1:n.*3336A>T
ENST00000584450.5:c.*125A>T	ENSP00000463714.1:n.*125A>T
ENST00000584601.5:c.3456A>T	ENSP00000462438.1:p.Lys1152Asn
NM_001005862.2:c.3456A>T , LRG_724t1:c.3456A>T	NP_001005862.1:p.Lys1152Asn
NM_001289936.1:c.3501A>T , LRG_724t4:c.3501A>T	NP_001276865.1:p.Lys1167Asn
NM_001289937.1:c.*125A>T	NP_001276866.1:n.*125A>T
NM_004448.3:c.3546A>T , LRG_724t2:c.3546A>T	NP_004439.2:p.Lys1182Asn
NR_110535.1:n.3870A>T
XM_024450641.1:c.3684A>T	XP_024306409.1:p.Lys1228Asn
XM_024450642.1:c.3639A>T	XP_024306410.1:p.Lys1213Asn
XM_024450643.1:c.3594A>T	XP_024306411.1:p.Lys1198Asn
NM_001005862.3:c.3456A>T	NP_001005862.1:p.Lys1152Asn
NM_001289936.2:c.3501A>T	NP_001276865.1:p.Lys1167Asn
NM_001289937.2:c.*125A>T	NP_001276866.1:n.*125A>T
NM_001382782.1:c.3456A>T	NP_001369711.1:p.Lys1152Asn
NM_001382783.1:c.3456A>T	NP_001369712.1:p.Lys1152Asn
NM_001382784.1:c.3663A>T	NP_001369713.1:p.Lys1221Asn
NM_001382785.1:c.3648A>T	NP_001369714.1:p.Lys1216Asn
NM_001382786.1:c.3627A>T	NP_001369715.1:p.Lys1209Asn
NM_001382787.1:c.3621A>T	NP_001369716.1:p.Lys1207Asn
NM_001382788.1:c.3576A>T	NP_001369717.1:p.Lys1192Asn
NM_001382789.1:c.3567A>T	NP_001369718.1:p.Lys1189Asn
NM_001382790.1:c.3543A>T	NP_001369719.1:p.Lys1181Asn
NM_001382791.1:c.3537A>T	NP_001369720.1:p.Lys1179Asn
NM_001382792.1:c.3510A>T	NP_001369721.1:p.Lys1170Asn
NM_001382793.1:c.3504A>T	NP_001369722.1:p.Lys1168Asn
NM_001382794.1:c.3504A>T	NP_001369723.1:p.Lys1168Asn
NM_001382795.1:c.3498A>T	NP_001369724.1:p.Lys1166Asn
NM_001382796.1:c.3459A>T	NP_001369725.1:p.Lys1153Asn
NM_001382797.1:c.3447A>T	NP_001369726.1:p.Lys1149Asn
NM_001382798.1:c.3390A>T	NP_001369727.1:p.Lys1130Asn
NM_001382799.1:c.3366A>T	NP_001369728.1:p.Lys1122Asn
NM_001382800.1:c.3360A>T	NP_001369729.1:p.Lys1120Asn
NM_001382801.1:c.3342A>T	NP_001369730.1:p.Lys1114Asn
NM_001382802.1:c.3288A>T	NP_001369731.1:p.Lys1096Asn
NM_001382803.1:c.*125A>T	NP_001369732.1:n.*125A>T
NM_001382804.1:c.2718A>T	NP_001369733.1:p.Lys906Asn
NM_001382805.1:c.2595A>T	NP_001369734.1:p.Lys865Asn
NM_001382806.1:c.2508A>T	NP_001369735.1:p.Lys836Asn
NM_004448.4:c.3546A>T MANE Select	NP_004439.2:p.Lys1182Asn
NR_110535.2:n.3784A>T