Canonical Allele Identifier: CA499890242

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37883713C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727460C>T , CM000679.2:g.39727460C>T	GRCh38
NC_000017.10:g.37883713C>T , CM000679.1:g.37883713C>T	GRCh37
NC_000017.9:g.35137239C>T	NCBI36
NG_007503.1:g.44321C>T , LRG_724:g.44321C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3325C>T MANE Select	ENSP00000269571.4:p.Leu1109=
ENST00000269571.9:c.3325C>T	ENSP00000269571.4:p.Leu1109=
ENST00000406381.6:c.3235C>T	ENSP00000385185.2:p.Leu1079=
ENST00000445658.6:c.2497C>T	ENSP00000404047.2:p.Leu833=
ENST00000541774.5:c.3280C>T	ENSP00000446466.1:p.Leu1094=
ENST00000578373.5:c.*3115C>T	ENSP00000463427.1:n.*3115C>T
ENST00000584450.5:c.3160-229C>T	ENSP00000463714.1:n.3160-229C>T
ENST00000584601.5:c.3235C>T	ENSP00000462438.1:p.Leu1079=
NM_001005862.2:c.3235C>T , LRG_724t1:c.3235C>T	NP_001005862.1:p.Leu1079=
NM_001289936.1:c.3280C>T , LRG_724t4:c.3280C>T	NP_001276865.1:p.Leu1094=
NM_001289937.1:c.3160-229C>T	NP_001276866.1:n.3160-229C>T
NM_004448.3:c.3325C>T , LRG_724t2:c.3325C>T	NP_004439.2:p.Leu1109=
NR_110535.1:n.3649C>T
XM_024450641.1:c.3463C>T	XP_024306409.1:p.Leu1155=
XM_024450642.1:c.3418C>T	XP_024306410.1:p.Leu1140=
XM_024450643.1:c.3373C>T	XP_024306411.1:p.Leu1125=
NM_001005862.3:c.3235C>T	NP_001005862.1:p.Leu1079=
NM_001289936.2:c.3280C>T	NP_001276865.1:p.Leu1094=
NM_001289937.2:c.3160-229C>T	NP_001276866.1:n.3160-229C>T
NM_001382782.1:c.3235C>T	NP_001369711.1:p.Leu1079=
NM_001382783.1:c.3235C>T	NP_001369712.1:p.Leu1079=
NM_001382784.1:c.3442C>T	NP_001369713.1:p.Leu1148=
NM_001382785.1:c.3427C>T	NP_001369714.1:p.Leu1143=
NM_001382786.1:c.3406C>T	NP_001369715.1:p.Leu1136=
NM_001382787.1:c.3400C>T	NP_001369716.1:p.Leu1134=
NM_001382788.1:c.3355C>T	NP_001369717.1:p.Leu1119=
NM_001382789.1:c.3346C>T	NP_001369718.1:p.Leu1116=
NM_001382790.1:c.3322C>T	NP_001369719.1:p.Leu1108=
NM_001382791.1:c.3316C>T	NP_001369720.1:p.Leu1106=
NM_001382792.1:c.3289C>T	NP_001369721.1:p.Leu1097=
NM_001382793.1:c.3283C>T	NP_001369722.1:p.Leu1095=
NM_001382794.1:c.3283C>T	NP_001369723.1:p.Leu1095=
NM_001382795.1:c.3277C>T	NP_001369724.1:p.Leu1093=
NM_001382796.1:c.3238C>T	NP_001369725.1:p.Leu1080=
NM_001382797.1:c.3226C>T	NP_001369726.1:p.Leu1076=
NM_001382798.1:c.3169C>T	NP_001369727.1:p.Leu1057=
NM_001382799.1:c.3145C>T	NP_001369728.1:p.Leu1049=
NM_001382800.1:c.3139C>T	NP_001369729.1:p.Leu1047=
NM_001382801.1:c.3121C>T	NP_001369730.1:p.Leu1041=
NM_001382802.1:c.3067C>T	NP_001369731.1:p.Leu1023=
NM_001382803.1:c.3118-229C>T	NP_001369732.1:n.3118-229C>T
NM_001382804.1:c.2497C>T	NP_001369733.1:p.Leu833=
NM_001382805.1:c.2374C>T	NP_001369734.1:p.Leu792=
NM_001382806.1:c.2287C>T	NP_001369735.1:p.Leu763=
NM_004448.4:c.3325C>T MANE Select	NP_004439.2:p.Leu1109=
NR_110535.2:n.3563C>T