Canonical Allele Identifier: CA399310621

Gene: ERBB2

Linked Data

• dbSNP Id: rs749154778
• gnomAD v4: 17-39727398-G-T
• MyVariant Identifiers: chr17:g.37883651G>T (hg19) ; chr17:g.39727398G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727398G>T , CM000679.2:g.39727398G>T	GRCh38
NC_000017.10:g.37883651G>T , CM000679.1:g.37883651G>T	GRCh37
NC_000017.9:g.35137177G>T	NCBI36
NG_007503.1:g.44259G>T , LRG_724:g.44259G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3263G>T MANE Select	ENSP00000269571.4:p.Gly1088Val
ENST00000269571.9:c.3263G>T	ENSP00000269571.4:p.Gly1088Val
ENST00000406381.6:c.3173G>T	ENSP00000385185.2:p.Gly1058Val
ENST00000445658.6:c.2435G>T	ENSP00000404047.2:p.Gly812Val
ENST00000541774.5:c.3218G>T	ENSP00000446466.1:p.Gly1073Val
ENST00000578373.5:c.*3053G>T	ENSP00000463427.1:n.*3053G>T
ENST00000584450.5:c.3160-291G>T	ENSP00000463714.1:n.3160-291G>T
ENST00000584601.5:c.3173G>T	ENSP00000462438.1:p.Gly1058Val
NM_001005862.2:c.3173G>T , LRG_724t1:c.3173G>T	NP_001005862.1:p.Gly1058Val
NM_001289936.1:c.3218G>T , LRG_724t4:c.3218G>T	NP_001276865.1:p.Gly1073Val
NM_001289937.1:c.3160-291G>T	NP_001276866.1:n.3160-291G>T
NM_004448.3:c.3263G>T , LRG_724t2:c.3263G>T	NP_004439.2:p.Gly1088Val
NR_110535.1:n.3587G>T
XM_024450641.1:c.3401G>T	XP_024306409.1:p.Gly1134Val
XM_024450642.1:c.3356G>T	XP_024306410.1:p.Gly1119Val
XM_024450643.1:c.3311G>T	XP_024306411.1:p.Gly1104Val
NM_001005862.3:c.3173G>T	NP_001005862.1:p.Gly1058Val
NM_001289936.2:c.3218G>T	NP_001276865.1:p.Gly1073Val
NM_001289937.2:c.3160-291G>T	NP_001276866.1:n.3160-291G>T
NM_001382782.1:c.3173G>T	NP_001369711.1:p.Gly1058Val
NM_001382783.1:c.3173G>T	NP_001369712.1:p.Gly1058Val
NM_001382784.1:c.3380G>T	NP_001369713.1:p.Gly1127Val
NM_001382785.1:c.3365G>T	NP_001369714.1:p.Gly1122Val
NM_001382786.1:c.3344G>T	NP_001369715.1:p.Gly1115Val
NM_001382787.1:c.3338G>T	NP_001369716.1:p.Gly1113Val
NM_001382788.1:c.3293G>T	NP_001369717.1:p.Gly1098Val
NM_001382789.1:c.3284G>T	NP_001369718.1:p.Gly1095Val
NM_001382790.1:c.3260G>T	NP_001369719.1:p.Gly1087Val
NM_001382791.1:c.3254G>T	NP_001369720.1:p.Gly1085Val
NM_001382792.1:c.3227G>T	NP_001369721.1:p.Gly1076Val
NM_001382793.1:c.3221G>T	NP_001369722.1:p.Gly1074Val
NM_001382794.1:c.3221G>T	NP_001369723.1:p.Gly1074Val
NM_001382795.1:c.3215G>T	NP_001369724.1:p.Gly1072Val
NM_001382796.1:c.3176G>T	NP_001369725.1:p.Gly1059Val
NM_001382797.1:c.3164G>T	NP_001369726.1:p.Gly1055Val
NM_001382798.1:c.3107G>T	NP_001369727.1:p.Gly1036Val
NM_001382799.1:c.3083G>T	NP_001369728.1:p.Gly1028Val
NM_001382800.1:c.3077G>T	NP_001369729.1:p.Gly1026Val
NM_001382801.1:c.3059G>T	NP_001369730.1:p.Gly1020Val
NM_001382802.1:c.3005G>T	NP_001369731.1:p.Gly1002Val
NM_001382803.1:c.3118-291G>T	NP_001369732.1:n.3118-291G>T
NM_001382804.1:c.2435G>T	NP_001369733.1:p.Gly812Val
NM_001382805.1:c.2312G>T	NP_001369734.1:p.Gly771Val
NM_001382806.1:c.2225G>T	NP_001369735.1:p.Gly742Val
NM_004448.4:c.3263G>T MANE Select	NP_004439.2:p.Gly1088Val
NR_110535.2:n.3501G>T