Canonical Allele Identifier: CA499671670

Gene: ERBB2

Linked Data

• dbSNP Id: rs770506053
• MyVariant Identifiers: chr17:g.37883682G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727429G>T , CM000679.2:g.39727429G>T	GRCh38
NC_000017.10:g.37883682G>T , CM000679.1:g.37883682G>T	GRCh37
NC_000017.9:g.35137208G>T	NCBI36
NG_007503.1:g.44290G>T , LRG_724:g.44290G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3294G>T MANE Select	ENSP00000269571.4:p.Leu1098=
ENST00000269571.9:c.3294G>T	ENSP00000269571.4:p.Leu1098=
ENST00000406381.6:c.3204G>T	ENSP00000385185.2:p.Leu1068=
ENST00000445658.6:c.2466G>T	ENSP00000404047.2:p.Leu822=
ENST00000541774.5:c.3249G>T	ENSP00000446466.1:p.Leu1083=
ENST00000578373.5:c.*3084G>T	ENSP00000463427.1:n.*3084G>T
ENST00000584450.5:c.3160-260G>T	ENSP00000463714.1:n.3160-260G>T
ENST00000584601.5:c.3204G>T	ENSP00000462438.1:p.Leu1068=
NM_001005862.2:c.3204G>T , LRG_724t1:c.3204G>T	NP_001005862.1:p.Leu1068=
NM_001289936.1:c.3249G>T , LRG_724t4:c.3249G>T	NP_001276865.1:p.Leu1083=
NM_001289937.1:c.3160-260G>T	NP_001276866.1:n.3160-260G>T
NM_004448.3:c.3294G>T , LRG_724t2:c.3294G>T	NP_004439.2:p.Leu1098=
NR_110535.1:n.3618G>T
XM_024450641.1:c.3432G>T	XP_024306409.1:p.Leu1144=
XM_024450642.1:c.3387G>T	XP_024306410.1:p.Leu1129=
XM_024450643.1:c.3342G>T	XP_024306411.1:p.Leu1114=
NM_001005862.3:c.3204G>T	NP_001005862.1:p.Leu1068=
NM_001289936.2:c.3249G>T	NP_001276865.1:p.Leu1083=
NM_001289937.2:c.3160-260G>T	NP_001276866.1:n.3160-260G>T
NM_001382782.1:c.3204G>T	NP_001369711.1:p.Leu1068=
NM_001382783.1:c.3204G>T	NP_001369712.1:p.Leu1068=
NM_001382784.1:c.3411G>T	NP_001369713.1:p.Leu1137=
NM_001382785.1:c.3396G>T	NP_001369714.1:p.Leu1132=
NM_001382786.1:c.3375G>T	NP_001369715.1:p.Leu1125=
NM_001382787.1:c.3369G>T	NP_001369716.1:p.Leu1123=
NM_001382788.1:c.3324G>T	NP_001369717.1:p.Leu1108=
NM_001382789.1:c.3315G>T	NP_001369718.1:p.Leu1105=
NM_001382790.1:c.3291G>T	NP_001369719.1:p.Leu1097=
NM_001382791.1:c.3285G>T	NP_001369720.1:p.Leu1095=
NM_001382792.1:c.3258G>T	NP_001369721.1:p.Leu1086=
NM_001382793.1:c.3252G>T	NP_001369722.1:p.Leu1084=
NM_001382794.1:c.3252G>T	NP_001369723.1:p.Leu1084=
NM_001382795.1:c.3246G>T	NP_001369724.1:p.Leu1082=
NM_001382796.1:c.3207G>T	NP_001369725.1:p.Leu1069=
NM_001382797.1:c.3195G>T	NP_001369726.1:p.Leu1065=
NM_001382798.1:c.3138G>T	NP_001369727.1:p.Leu1046=
NM_001382799.1:c.3114G>T	NP_001369728.1:p.Leu1038=
NM_001382800.1:c.3108G>T	NP_001369729.1:p.Leu1036=
NM_001382801.1:c.3090G>T	NP_001369730.1:p.Leu1030=
NM_001382802.1:c.3036G>T	NP_001369731.1:p.Leu1012=
NM_001382803.1:c.3118-260G>T	NP_001369732.1:n.3118-260G>T
NM_001382804.1:c.2466G>T	NP_001369733.1:p.Leu822=
NM_001382805.1:c.2343G>T	NP_001369734.1:p.Leu781=
NM_001382806.1:c.2256G>T	NP_001369735.1:p.Leu752=
NM_004448.4:c.3294G>T MANE Select	NP_004439.2:p.Leu1098=
NR_110535.2:n.3532G>T