Canonical Allele Identifier: CA499671651

Gene: ERBB2

Linked Data

• dbSNP Id: rs2059835981
• MyVariant Identifiers: chr17:g.37883658G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727405G>T , CM000679.2:g.39727405G>T	GRCh38
NC_000017.10:g.37883658G>T , CM000679.1:g.37883658G>T	GRCh37
NC_000017.9:g.35137184G>T	NCBI36
NG_007503.1:g.44266G>T , LRG_724:g.44266G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3270G>T MANE Select	ENSP00000269571.4:p.Leu1090=
ENST00000269571.9:c.3270G>T	ENSP00000269571.4:p.Leu1090=
ENST00000406381.6:c.3180G>T	ENSP00000385185.2:p.Leu1060=
ENST00000445658.6:c.2442G>T	ENSP00000404047.2:p.Leu814=
ENST00000541774.5:c.3225G>T	ENSP00000446466.1:p.Leu1075=
ENST00000578373.5:c.*3060G>T	ENSP00000463427.1:n.*3060G>T
ENST00000584450.5:c.3160-284G>T	ENSP00000463714.1:n.3160-284G>T
ENST00000584601.5:c.3180G>T	ENSP00000462438.1:p.Leu1060=
NM_001005862.2:c.3180G>T , LRG_724t1:c.3180G>T	NP_001005862.1:p.Leu1060=
NM_001289936.1:c.3225G>T , LRG_724t4:c.3225G>T	NP_001276865.1:p.Leu1075=
NM_001289937.1:c.3160-284G>T	NP_001276866.1:n.3160-284G>T
NM_004448.3:c.3270G>T , LRG_724t2:c.3270G>T	NP_004439.2:p.Leu1090=
NR_110535.1:n.3594G>T
XM_024450641.1:c.3408G>T	XP_024306409.1:p.Leu1136=
XM_024450642.1:c.3363G>T	XP_024306410.1:p.Leu1121=
XM_024450643.1:c.3318G>T	XP_024306411.1:p.Leu1106=
NM_001005862.3:c.3180G>T	NP_001005862.1:p.Leu1060=
NM_001289936.2:c.3225G>T	NP_001276865.1:p.Leu1075=
NM_001289937.2:c.3160-284G>T	NP_001276866.1:n.3160-284G>T
NM_001382782.1:c.3180G>T	NP_001369711.1:p.Leu1060=
NM_001382783.1:c.3180G>T	NP_001369712.1:p.Leu1060=
NM_001382784.1:c.3387G>T	NP_001369713.1:p.Leu1129=
NM_001382785.1:c.3372G>T	NP_001369714.1:p.Leu1124=
NM_001382786.1:c.3351G>T	NP_001369715.1:p.Leu1117=
NM_001382787.1:c.3345G>T	NP_001369716.1:p.Leu1115=
NM_001382788.1:c.3300G>T	NP_001369717.1:p.Leu1100=
NM_001382789.1:c.3291G>T	NP_001369718.1:p.Leu1097=
NM_001382790.1:c.3267G>T	NP_001369719.1:p.Leu1089=
NM_001382791.1:c.3261G>T	NP_001369720.1:p.Leu1087=
NM_001382792.1:c.3234G>T	NP_001369721.1:p.Leu1078=
NM_001382793.1:c.3228G>T	NP_001369722.1:p.Leu1076=
NM_001382794.1:c.3228G>T	NP_001369723.1:p.Leu1076=
NM_001382795.1:c.3222G>T	NP_001369724.1:p.Leu1074=
NM_001382796.1:c.3183G>T	NP_001369725.1:p.Leu1061=
NM_001382797.1:c.3171G>T	NP_001369726.1:p.Leu1057=
NM_001382798.1:c.3114G>T	NP_001369727.1:p.Leu1038=
NM_001382799.1:c.3090G>T	NP_001369728.1:p.Leu1030=
NM_001382800.1:c.3084G>T	NP_001369729.1:p.Leu1028=
NM_001382801.1:c.3066G>T	NP_001369730.1:p.Leu1022=
NM_001382802.1:c.3012G>T	NP_001369731.1:p.Leu1004=
NM_001382803.1:c.3118-284G>T	NP_001369732.1:n.3118-284G>T
NM_001382804.1:c.2442G>T	NP_001369733.1:p.Leu814=
NM_001382805.1:c.2319G>T	NP_001369734.1:p.Leu773=
NM_001382806.1:c.2232G>T	NP_001369735.1:p.Leu744=
NM_004448.4:c.3270G>T MANE Select	NP_004439.2:p.Leu1090=
NR_110535.2:n.3508G>T