Canonical Allele Identifier: CA499671675

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37883691C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727438C>T , CM000679.2:g.39727438C>T	GRCh38
NC_000017.10:g.37883691C>T , CM000679.1:g.37883691C>T	GRCh37
NC_000017.9:g.35137217C>T	NCBI36
NG_007503.1:g.44299C>T , LRG_724:g.44299C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3303C>T MANE Select	ENSP00000269571.4:p.Leu1101=
ENST00000269571.9:c.3303C>T	ENSP00000269571.4:p.Leu1101=
ENST00000406381.6:c.3213C>T	ENSP00000385185.2:p.Leu1071=
ENST00000445658.6:c.2475C>T	ENSP00000404047.2:p.Leu825=
ENST00000541774.5:c.3258C>T	ENSP00000446466.1:p.Leu1086=
ENST00000578373.5:c.*3093C>T	ENSP00000463427.1:n.*3093C>T
ENST00000584450.5:c.3160-251C>T	ENSP00000463714.1:n.3160-251C>T
ENST00000584601.5:c.3213C>T	ENSP00000462438.1:p.Leu1071=
NM_001005862.2:c.3213C>T , LRG_724t1:c.3213C>T	NP_001005862.1:p.Leu1071=
NM_001289936.1:c.3258C>T , LRG_724t4:c.3258C>T	NP_001276865.1:p.Leu1086=
NM_001289937.1:c.3160-251C>T	NP_001276866.1:n.3160-251C>T
NM_004448.3:c.3303C>T , LRG_724t2:c.3303C>T	NP_004439.2:p.Leu1101=
NR_110535.1:n.3627C>T
XM_024450641.1:c.3441C>T	XP_024306409.1:p.Leu1147=
XM_024450642.1:c.3396C>T	XP_024306410.1:p.Leu1132=
XM_024450643.1:c.3351C>T	XP_024306411.1:p.Leu1117=
NM_001005862.3:c.3213C>T	NP_001005862.1:p.Leu1071=
NM_001289936.2:c.3258C>T	NP_001276865.1:p.Leu1086=
NM_001289937.2:c.3160-251C>T	NP_001276866.1:n.3160-251C>T
NM_001382782.1:c.3213C>T	NP_001369711.1:p.Leu1071=
NM_001382783.1:c.3213C>T	NP_001369712.1:p.Leu1071=
NM_001382784.1:c.3420C>T	NP_001369713.1:p.Leu1140=
NM_001382785.1:c.3405C>T	NP_001369714.1:p.Leu1135=
NM_001382786.1:c.3384C>T	NP_001369715.1:p.Leu1128=
NM_001382787.1:c.3378C>T	NP_001369716.1:p.Leu1126=
NM_001382788.1:c.3333C>T	NP_001369717.1:p.Leu1111=
NM_001382789.1:c.3324C>T	NP_001369718.1:p.Leu1108=
NM_001382790.1:c.3300C>T	NP_001369719.1:p.Leu1100=
NM_001382791.1:c.3294C>T	NP_001369720.1:p.Leu1098=
NM_001382792.1:c.3267C>T	NP_001369721.1:p.Leu1089=
NM_001382793.1:c.3261C>T	NP_001369722.1:p.Leu1087=
NM_001382794.1:c.3261C>T	NP_001369723.1:p.Leu1087=
NM_001382795.1:c.3255C>T	NP_001369724.1:p.Leu1085=
NM_001382796.1:c.3216C>T	NP_001369725.1:p.Leu1072=
NM_001382797.1:c.3204C>T	NP_001369726.1:p.Leu1068=
NM_001382798.1:c.3147C>T	NP_001369727.1:p.Leu1049=
NM_001382799.1:c.3123C>T	NP_001369728.1:p.Leu1041=
NM_001382800.1:c.3117C>T	NP_001369729.1:p.Leu1039=
NM_001382801.1:c.3099C>T	NP_001369730.1:p.Leu1033=
NM_001382802.1:c.3045C>T	NP_001369731.1:p.Leu1015=
NM_001382803.1:c.3118-251C>T	NP_001369732.1:n.3118-251C>T
NM_001382804.1:c.2475C>T	NP_001369733.1:p.Leu825=
NM_001382805.1:c.2352C>T	NP_001369734.1:p.Leu784=
NM_001382806.1:c.2265C>T	NP_001369735.1:p.Leu755=
NM_004448.4:c.3303C>T MANE Select	NP_004439.2:p.Leu1101=
NR_110535.2:n.3541C>T