Canonical Allele Identifier: CA399313361

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143298503
• MyVariant Identifiers: chr17:g.37884059A>T (hg19) ; chr17:g.39727806A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727806A>T , CM000679.2:g.39727806A>T	GRCh38
NC_000017.10:g.37884059A>T , CM000679.1:g.37884059A>T	GRCh37
NC_000017.9:g.35137585A>T	NCBI36
NG_007503.1:g.44667A>T , LRG_724:g.44667A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3530A>T MANE Select	ENSP00000269571.4:p.Lys1177Met
ENST00000269571.9:c.3530A>T	ENSP00000269571.4:p.Lys1177Met
ENST00000406381.6:c.3440A>T	ENSP00000385185.2:p.Lys1147Met
ENST00000445658.6:c.2702A>T	ENSP00000404047.2:p.Lys901Met
ENST00000541774.5:c.3485A>T	ENSP00000446466.1:p.Lys1162Met
ENST00000578373.5:c.*3320A>T	ENSP00000463427.1:n.*3320A>T
ENST00000584450.5:c.*109A>T	ENSP00000463714.1:n.*109A>T
ENST00000584601.5:c.3440A>T	ENSP00000462438.1:p.Lys1147Met
NM_001005862.2:c.3440A>T , LRG_724t1:c.3440A>T	NP_001005862.1:p.Lys1147Met
NM_001289936.1:c.3485A>T , LRG_724t4:c.3485A>T	NP_001276865.1:p.Lys1162Met
NM_001289937.1:c.*109A>T	NP_001276866.1:n.*109A>T
NM_004448.3:c.3530A>T , LRG_724t2:c.3530A>T	NP_004439.2:p.Lys1177Met
NR_110535.1:n.3854A>T
XM_024450641.1:c.3668A>T	XP_024306409.1:p.Lys1223Met
XM_024450642.1:c.3623A>T	XP_024306410.1:p.Lys1208Met
XM_024450643.1:c.3578A>T	XP_024306411.1:p.Lys1193Met
NM_001005862.3:c.3440A>T	NP_001005862.1:p.Lys1147Met
NM_001289936.2:c.3485A>T	NP_001276865.1:p.Lys1162Met
NM_001289937.2:c.*109A>T	NP_001276866.1:n.*109A>T
NM_001382782.1:c.3440A>T	NP_001369711.1:p.Lys1147Met
NM_001382783.1:c.3440A>T	NP_001369712.1:p.Lys1147Met
NM_001382784.1:c.3647A>T	NP_001369713.1:p.Lys1216Met
NM_001382785.1:c.3632A>T	NP_001369714.1:p.Lys1211Met
NM_001382786.1:c.3611A>T	NP_001369715.1:p.Lys1204Met
NM_001382787.1:c.3605A>T	NP_001369716.1:p.Lys1202Met
NM_001382788.1:c.3560A>T	NP_001369717.1:p.Lys1187Met
NM_001382789.1:c.3551A>T	NP_001369718.1:p.Lys1184Met
NM_001382790.1:c.3527A>T	NP_001369719.1:p.Lys1176Met
NM_001382791.1:c.3521A>T	NP_001369720.1:p.Lys1174Met
NM_001382792.1:c.3494A>T	NP_001369721.1:p.Lys1165Met
NM_001382793.1:c.3488A>T	NP_001369722.1:p.Lys1163Met
NM_001382794.1:c.3488A>T	NP_001369723.1:p.Lys1163Met
NM_001382795.1:c.3482A>T	NP_001369724.1:p.Lys1161Met
NM_001382796.1:c.3443A>T	NP_001369725.1:p.Lys1148Met
NM_001382797.1:c.3431A>T	NP_001369726.1:p.Lys1144Met
NM_001382798.1:c.3374A>T	NP_001369727.1:p.Lys1125Met
NM_001382799.1:c.3350A>T	NP_001369728.1:p.Lys1117Met
NM_001382800.1:c.3344A>T	NP_001369729.1:p.Lys1115Met
NM_001382801.1:c.3326A>T	NP_001369730.1:p.Lys1109Met
NM_001382802.1:c.3272A>T	NP_001369731.1:p.Lys1091Met
NM_001382803.1:c.*109A>T	NP_001369732.1:n.*109A>T
NM_001382804.1:c.2702A>T	NP_001369733.1:p.Lys901Met
NM_001382805.1:c.2579A>T	NP_001369734.1:p.Lys860Met
NM_001382806.1:c.2492A>T	NP_001369735.1:p.Lys831Met
NM_004448.4:c.3530A>T MANE Select	NP_004439.2:p.Lys1177Met
NR_110535.2:n.3768A>T