Canonical Allele Identifier: CA499890654

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37884030G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727777G>T , CM000679.2:g.39727777G>T	GRCh38
NC_000017.10:g.37884030G>T , CM000679.1:g.37884030G>T	GRCh37
NC_000017.9:g.35137556G>T	NCBI36
NG_007503.1:g.44638G>T , LRG_724:g.44638G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3501G>T MANE Select	ENSP00000269571.4:p.Leu1167=
ENST00000269571.9:c.3501G>T	ENSP00000269571.4:p.Leu1167=
ENST00000406381.6:c.3411G>T	ENSP00000385185.2:p.Leu1137=
ENST00000445658.6:c.2673G>T	ENSP00000404047.2:p.Leu891=
ENST00000541774.5:c.3456G>T	ENSP00000446466.1:p.Leu1152=
ENST00000578373.5:c.*3291G>T	ENSP00000463427.1:n.*3291G>T
ENST00000584450.5:c.*80G>T	ENSP00000463714.1:n.*80G>T
ENST00000584601.5:c.3411G>T	ENSP00000462438.1:p.Leu1137=
NM_001005862.2:c.3411G>T , LRG_724t1:c.3411G>T	NP_001005862.1:p.Leu1137=
NM_001289936.1:c.3456G>T , LRG_724t4:c.3456G>T	NP_001276865.1:p.Leu1152=
NM_001289937.1:c.*80G>T	NP_001276866.1:n.*80G>T
NM_004448.3:c.3501G>T , LRG_724t2:c.3501G>T	NP_004439.2:p.Leu1167=
NR_110535.1:n.3825G>T
XM_024450641.1:c.3639G>T	XP_024306409.1:p.Leu1213=
XM_024450642.1:c.3594G>T	XP_024306410.1:p.Leu1198=
XM_024450643.1:c.3549G>T	XP_024306411.1:p.Leu1183=
NM_001005862.3:c.3411G>T	NP_001005862.1:p.Leu1137=
NM_001289936.2:c.3456G>T	NP_001276865.1:p.Leu1152=
NM_001289937.2:c.*80G>T	NP_001276866.1:n.*80G>T
NM_001382782.1:c.3411G>T	NP_001369711.1:p.Leu1137=
NM_001382783.1:c.3411G>T	NP_001369712.1:p.Leu1137=
NM_001382784.1:c.3618G>T	NP_001369713.1:p.Leu1206=
NM_001382785.1:c.3603G>T	NP_001369714.1:p.Leu1201=
NM_001382786.1:c.3582G>T	NP_001369715.1:p.Leu1194=
NM_001382787.1:c.3576G>T	NP_001369716.1:p.Leu1192=
NM_001382788.1:c.3531G>T	NP_001369717.1:p.Leu1177=
NM_001382789.1:c.3522G>T	NP_001369718.1:p.Leu1174=
NM_001382790.1:c.3498G>T	NP_001369719.1:p.Leu1166=
NM_001382791.1:c.3492G>T	NP_001369720.1:p.Leu1164=
NM_001382792.1:c.3465G>T	NP_001369721.1:p.Leu1155=
NM_001382793.1:c.3459G>T	NP_001369722.1:p.Leu1153=
NM_001382794.1:c.3459G>T	NP_001369723.1:p.Leu1153=
NM_001382795.1:c.3453G>T	NP_001369724.1:p.Leu1151=
NM_001382796.1:c.3414G>T	NP_001369725.1:p.Leu1138=
NM_001382797.1:c.3402G>T	NP_001369726.1:p.Leu1134=
NM_001382798.1:c.3345G>T	NP_001369727.1:p.Leu1115=
NM_001382799.1:c.3321G>T	NP_001369728.1:p.Leu1107=
NM_001382800.1:c.3315G>T	NP_001369729.1:p.Leu1105=
NM_001382801.1:c.3297G>T	NP_001369730.1:p.Leu1099=
NM_001382802.1:c.3243G>T	NP_001369731.1:p.Leu1081=
NM_001382803.1:c.*80G>T	NP_001369732.1:n.*80G>T
NM_001382804.1:c.2673G>T	NP_001369733.1:p.Leu891=
NM_001382805.1:c.2550G>T	NP_001369734.1:p.Leu850=
NM_001382806.1:c.2463G>T	NP_001369735.1:p.Leu821=
NM_004448.4:c.3501G>T MANE Select	NP_004439.2:p.Leu1167=
NR_110535.2:n.3739G>T