Canonical Allele Identifier: CA499890244

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143251116
• MyVariant Identifiers: chr17:g.37883715A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727462A>G , CM000679.2:g.39727462A>G	GRCh38
NC_000017.10:g.37883715A>G , CM000679.1:g.37883715A>G	GRCh37
NC_000017.9:g.35137241A>G	NCBI36
NG_007503.1:g.44323A>G , LRG_724:g.44323A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3327A>G MANE Select	ENSP00000269571.4:p.Leu1109=
ENST00000269571.9:c.3327A>G	ENSP00000269571.4:p.Leu1109=
ENST00000406381.6:c.3237A>G	ENSP00000385185.2:p.Leu1079=
ENST00000445658.6:c.2499A>G	ENSP00000404047.2:p.Leu833=
ENST00000541774.5:c.3282A>G	ENSP00000446466.1:p.Leu1094=
ENST00000578373.5:c.*3117A>G	ENSP00000463427.1:n.*3117A>G
ENST00000584450.5:c.3160-227A>G	ENSP00000463714.1:n.3160-227A>G
ENST00000584601.5:c.3237A>G	ENSP00000462438.1:p.Leu1079=
NM_001005862.2:c.3237A>G , LRG_724t1:c.3237A>G	NP_001005862.1:p.Leu1079=
NM_001289936.1:c.3282A>G , LRG_724t4:c.3282A>G	NP_001276865.1:p.Leu1094=
NM_001289937.1:c.3160-227A>G	NP_001276866.1:n.3160-227A>G
NM_004448.3:c.3327A>G , LRG_724t2:c.3327A>G	NP_004439.2:p.Leu1109=
NR_110535.1:n.3651A>G
XM_024450641.1:c.3465A>G	XP_024306409.1:p.Leu1155=
XM_024450642.1:c.3420A>G	XP_024306410.1:p.Leu1140=
XM_024450643.1:c.3375A>G	XP_024306411.1:p.Leu1125=
NM_001005862.3:c.3237A>G	NP_001005862.1:p.Leu1079=
NM_001289936.2:c.3282A>G	NP_001276865.1:p.Leu1094=
NM_001289937.2:c.3160-227A>G	NP_001276866.1:n.3160-227A>G
NM_001382782.1:c.3237A>G	NP_001369711.1:p.Leu1079=
NM_001382783.1:c.3237A>G	NP_001369712.1:p.Leu1079=
NM_001382784.1:c.3444A>G	NP_001369713.1:p.Leu1148=
NM_001382785.1:c.3429A>G	NP_001369714.1:p.Leu1143=
NM_001382786.1:c.3408A>G	NP_001369715.1:p.Leu1136=
NM_001382787.1:c.3402A>G	NP_001369716.1:p.Leu1134=
NM_001382788.1:c.3357A>G	NP_001369717.1:p.Leu1119=
NM_001382789.1:c.3348A>G	NP_001369718.1:p.Leu1116=
NM_001382790.1:c.3324A>G	NP_001369719.1:p.Leu1108=
NM_001382791.1:c.3318A>G	NP_001369720.1:p.Leu1106=
NM_001382792.1:c.3291A>G	NP_001369721.1:p.Leu1097=
NM_001382793.1:c.3285A>G	NP_001369722.1:p.Leu1095=
NM_001382794.1:c.3285A>G	NP_001369723.1:p.Leu1095=
NM_001382795.1:c.3279A>G	NP_001369724.1:p.Leu1093=
NM_001382796.1:c.3240A>G	NP_001369725.1:p.Leu1080=
NM_001382797.1:c.3228A>G	NP_001369726.1:p.Leu1076=
NM_001382798.1:c.3171A>G	NP_001369727.1:p.Leu1057=
NM_001382799.1:c.3147A>G	NP_001369728.1:p.Leu1049=
NM_001382800.1:c.3141A>G	NP_001369729.1:p.Leu1047=
NM_001382801.1:c.3123A>G	NP_001369730.1:p.Leu1041=
NM_001382802.1:c.3069A>G	NP_001369731.1:p.Leu1023=
NM_001382803.1:c.3118-227A>G	NP_001369732.1:n.3118-227A>G
NM_001382804.1:c.2499A>G	NP_001369733.1:p.Leu833=
NM_001382805.1:c.2376A>G	NP_001369734.1:p.Leu792=
NM_001382806.1:c.2289A>G	NP_001369735.1:p.Leu763=
NM_004448.4:c.3327A>G MANE Select	NP_004439.2:p.Leu1109=
NR_110535.2:n.3565A>G