Canonical Allele Identifier: CA399313149

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37884029T>G (hg19) ; chr17:g.39727776T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727776T>G , CM000679.2:g.39727776T>G	GRCh38
NC_000017.10:g.37884029T>G , CM000679.1:g.37884029T>G	GRCh37
NC_000017.9:g.35137555T>G	NCBI36
NG_007503.1:g.44637T>G , LRG_724:g.44637T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3500T>G MANE Select	ENSP00000269571.4:p.Leu1167Arg
ENST00000269571.9:c.3500T>G	ENSP00000269571.4:p.Leu1167Arg
ENST00000406381.6:c.3410T>G	ENSP00000385185.2:p.Leu1137Arg
ENST00000445658.6:c.2672T>G	ENSP00000404047.2:p.Leu891Arg
ENST00000541774.5:c.3455T>G	ENSP00000446466.1:p.Leu1152Arg
ENST00000578373.5:c.*3290T>G	ENSP00000463427.1:n.*3290T>G
ENST00000584450.5:c.*79T>G	ENSP00000463714.1:n.*79T>G
ENST00000584601.5:c.3410T>G	ENSP00000462438.1:p.Leu1137Arg
NM_001005862.2:c.3410T>G , LRG_724t1:c.3410T>G	NP_001005862.1:p.Leu1137Arg
NM_001289936.1:c.3455T>G , LRG_724t4:c.3455T>G	NP_001276865.1:p.Leu1152Arg
NM_001289937.1:c.*79T>G	NP_001276866.1:n.*79T>G
NM_004448.3:c.3500T>G , LRG_724t2:c.3500T>G	NP_004439.2:p.Leu1167Arg
NR_110535.1:n.3824T>G
XM_024450641.1:c.3638T>G	XP_024306409.1:p.Leu1213Arg
XM_024450642.1:c.3593T>G	XP_024306410.1:p.Leu1198Arg
XM_024450643.1:c.3548T>G	XP_024306411.1:p.Leu1183Arg
NM_001005862.3:c.3410T>G	NP_001005862.1:p.Leu1137Arg
NM_001289936.2:c.3455T>G	NP_001276865.1:p.Leu1152Arg
NM_001289937.2:c.*79T>G	NP_001276866.1:n.*79T>G
NM_001382782.1:c.3410T>G	NP_001369711.1:p.Leu1137Arg
NM_001382783.1:c.3410T>G	NP_001369712.1:p.Leu1137Arg
NM_001382784.1:c.3617T>G	NP_001369713.1:p.Leu1206Arg
NM_001382785.1:c.3602T>G	NP_001369714.1:p.Leu1201Arg
NM_001382786.1:c.3581T>G	NP_001369715.1:p.Leu1194Arg
NM_001382787.1:c.3575T>G	NP_001369716.1:p.Leu1192Arg
NM_001382788.1:c.3530T>G	NP_001369717.1:p.Leu1177Arg
NM_001382789.1:c.3521T>G	NP_001369718.1:p.Leu1174Arg
NM_001382790.1:c.3497T>G	NP_001369719.1:p.Leu1166Arg
NM_001382791.1:c.3491T>G	NP_001369720.1:p.Leu1164Arg
NM_001382792.1:c.3464T>G	NP_001369721.1:p.Leu1155Arg
NM_001382793.1:c.3458T>G	NP_001369722.1:p.Leu1153Arg
NM_001382794.1:c.3458T>G	NP_001369723.1:p.Leu1153Arg
NM_001382795.1:c.3452T>G	NP_001369724.1:p.Leu1151Arg
NM_001382796.1:c.3413T>G	NP_001369725.1:p.Leu1138Arg
NM_001382797.1:c.3401T>G	NP_001369726.1:p.Leu1134Arg
NM_001382798.1:c.3344T>G	NP_001369727.1:p.Leu1115Arg
NM_001382799.1:c.3320T>G	NP_001369728.1:p.Leu1107Arg
NM_001382800.1:c.3314T>G	NP_001369729.1:p.Leu1105Arg
NM_001382801.1:c.3296T>G	NP_001369730.1:p.Leu1099Arg
NM_001382802.1:c.3242T>G	NP_001369731.1:p.Leu1081Arg
NM_001382803.1:c.*79T>G	NP_001369732.1:n.*79T>G
NM_001382804.1:c.2672T>G	NP_001369733.1:p.Leu891Arg
NM_001382805.1:c.2549T>G	NP_001369734.1:p.Leu850Arg
NM_001382806.1:c.2462T>G	NP_001369735.1:p.Leu821Arg
NM_004448.4:c.3500T>G MANE Select	NP_004439.2:p.Leu1167Arg
NR_110535.2:n.3738T>G