Canonical Allele Identifier: CA499670874

Gene: ERBB2

Linked Data

• dbSNP Id: rs2145849497
• MyVariant Identifiers: chr17:g.37881041G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39724788G>T , CM000679.2:g.39724788G>T	GRCh38
NC_000017.10:g.37881041G>T , CM000679.1:g.37881041G>T	GRCh37
NC_000017.9:g.35134567G>T	NCBI36
NG_007503.1:g.41649G>T , LRG_724:g.41649G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2370G>T MANE Select	ENSP00000269571.4:p.Leu790=
ENST00000269571.9:c.2370G>T	ENSP00000269571.4:p.Leu790=
ENST00000406381.6:c.2280G>T	ENSP00000385185.2:p.Leu760=
ENST00000445658.6:c.1542G>T	ENSP00000404047.2:p.Leu514=
ENST00000541774.5:c.2325G>T	ENSP00000446466.1:p.Leu775=
ENST00000578373.5:c.*2160G>T	ENSP00000463427.1:n.*2160G>T
ENST00000580074.1:c.476G>T
ENST00000583038.5:n.3504G>T
ENST00000584450.5:c.2370G>T	ENSP00000463714.1:p.Leu790=
ENST00000584601.5:c.2280G>T	ENSP00000462438.1:p.Leu760=
NM_001005862.2:c.2280G>T , LRG_724t1:c.2280G>T	NP_001005862.1:p.Leu760=
NM_001289936.1:c.2325G>T , LRG_724t4:c.2325G>T	NP_001276865.1:p.Leu775=
NM_001289937.1:c.2370G>T	NP_001276866.1:p.Leu790=
NM_004448.3:c.2370G>T , LRG_724t2:c.2370G>T	NP_004439.2:p.Leu790=
NR_110535.1:n.2694G>T
XM_024450641.1:c.2508G>T	XP_024306409.1:p.Leu836=
XM_024450642.1:c.2463G>T	XP_024306410.1:p.Leu821=
XM_024450643.1:c.2418G>T	XP_024306411.1:p.Leu806=
NM_001005862.3:c.2280G>T	NP_001005862.1:p.Leu760=
NM_001289936.2:c.2325G>T	NP_001276865.1:p.Leu775=
NM_001289937.2:c.2370G>T	NP_001276866.1:p.Leu790=
NM_001382782.1:c.2280G>T	NP_001369711.1:p.Leu760=
NM_001382783.1:c.2280G>T	NP_001369712.1:p.Leu760=
NM_001382784.1:c.2487G>T	NP_001369713.1:p.Leu829=
NM_001382785.1:c.2472G>T	NP_001369714.1:p.Leu824=
NM_001382786.1:c.2451G>T	NP_001369715.1:p.Leu817=
NM_001382787.1:c.2445G>T	NP_001369716.1:p.Leu815=
NM_001382788.1:c.2400G>T	NP_001369717.1:p.Leu800=
NM_001382789.1:c.2391G>T	NP_001369718.1:p.Leu797=
NM_001382790.1:c.2367G>T	NP_001369719.1:p.Leu789=
NM_001382791.1:c.2361G>T	NP_001369720.1:p.Leu787=
NM_001382792.1:c.2334G>T	NP_001369721.1:p.Leu778=
NM_001382793.1:c.2328G>T	NP_001369722.1:p.Leu776=
NM_001382794.1:c.2328G>T	NP_001369723.1:p.Leu776=
NM_001382795.1:c.2322G>T	NP_001369724.1:p.Leu774=
NM_001382796.1:c.2370G>T	NP_001369725.1:p.Leu790=
NM_001382797.1:c.2271G>T	NP_001369726.1:p.Leu757=
NM_001382798.1:c.2370G>T	NP_001369727.1:p.Leu790=
NM_001382799.1:c.2190G>T	NP_001369728.1:p.Leu730=
NM_001382800.1:c.2308-261G>T	NP_001369729.1:n.2308-261G>T
NM_001382801.1:c.2322G>T	NP_001369730.1:p.Leu774=
NM_001382802.1:c.2112G>T	NP_001369731.1:p.Leu704=
NM_001382803.1:c.2328G>T	NP_001369732.1:p.Leu776=
NM_001382804.1:c.1542G>T	NP_001369733.1:p.Leu514=
NM_001382805.1:c.2208+1128G>T	NP_001369734.1:n.2208+1128G>T
NM_001382806.1:c.1332G>T	NP_001369735.1:p.Leu444=
NM_004448.4:c.2370G>T MANE Select	NP_004439.2:p.Leu790=
NR_110535.2:n.2608G>T