Canonical Allele Identifier: CA399310910

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143248685
• MyVariant Identifiers: chr17:g.37883695A>G (hg19) ; chr17:g.39727442A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727442A>G , CM000679.2:g.39727442A>G	GRCh38
NC_000017.10:g.37883695A>G , CM000679.1:g.37883695A>G	GRCh37
NC_000017.9:g.35137221A>G	NCBI36
NG_007503.1:g.44303A>G , LRG_724:g.44303A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3307A>G MANE Select	ENSP00000269571.4:p.Thr1103Ala
ENST00000269571.9:c.3307A>G	ENSP00000269571.4:p.Thr1103Ala
ENST00000406381.6:c.3217A>G	ENSP00000385185.2:p.Thr1073Ala
ENST00000445658.6:c.2479A>G	ENSP00000404047.2:p.Thr827Ala
ENST00000541774.5:c.3262A>G	ENSP00000446466.1:p.Thr1088Ala
ENST00000578373.5:c.*3097A>G	ENSP00000463427.1:n.*3097A>G
ENST00000584450.5:c.3160-247A>G	ENSP00000463714.1:n.3160-247A>G
ENST00000584601.5:c.3217A>G	ENSP00000462438.1:p.Thr1073Ala
NM_001005862.2:c.3217A>G , LRG_724t1:c.3217A>G	NP_001005862.1:p.Thr1073Ala
NM_001289936.1:c.3262A>G , LRG_724t4:c.3262A>G	NP_001276865.1:p.Thr1088Ala
NM_001289937.1:c.3160-247A>G	NP_001276866.1:n.3160-247A>G
NM_004448.3:c.3307A>G , LRG_724t2:c.3307A>G	NP_004439.2:p.Thr1103Ala
NR_110535.1:n.3631A>G
XM_024450641.1:c.3445A>G	XP_024306409.1:p.Thr1149Ala
XM_024450642.1:c.3400A>G	XP_024306410.1:p.Thr1134Ala
XM_024450643.1:c.3355A>G	XP_024306411.1:p.Thr1119Ala
NM_001005862.3:c.3217A>G	NP_001005862.1:p.Thr1073Ala
NM_001289936.2:c.3262A>G	NP_001276865.1:p.Thr1088Ala
NM_001289937.2:c.3160-247A>G	NP_001276866.1:n.3160-247A>G
NM_001382782.1:c.3217A>G	NP_001369711.1:p.Thr1073Ala
NM_001382783.1:c.3217A>G	NP_001369712.1:p.Thr1073Ala
NM_001382784.1:c.3424A>G	NP_001369713.1:p.Thr1142Ala
NM_001382785.1:c.3409A>G	NP_001369714.1:p.Thr1137Ala
NM_001382786.1:c.3388A>G	NP_001369715.1:p.Thr1130Ala
NM_001382787.1:c.3382A>G	NP_001369716.1:p.Thr1128Ala
NM_001382788.1:c.3337A>G	NP_001369717.1:p.Thr1113Ala
NM_001382789.1:c.3328A>G	NP_001369718.1:p.Thr1110Ala
NM_001382790.1:c.3304A>G	NP_001369719.1:p.Thr1102Ala
NM_001382791.1:c.3298A>G	NP_001369720.1:p.Thr1100Ala
NM_001382792.1:c.3271A>G	NP_001369721.1:p.Thr1091Ala
NM_001382793.1:c.3265A>G	NP_001369722.1:p.Thr1089Ala
NM_001382794.1:c.3265A>G	NP_001369723.1:p.Thr1089Ala
NM_001382795.1:c.3259A>G	NP_001369724.1:p.Thr1087Ala
NM_001382796.1:c.3220A>G	NP_001369725.1:p.Thr1074Ala
NM_001382797.1:c.3208A>G	NP_001369726.1:p.Thr1070Ala
NM_001382798.1:c.3151A>G	NP_001369727.1:p.Thr1051Ala
NM_001382799.1:c.3127A>G	NP_001369728.1:p.Thr1043Ala
NM_001382800.1:c.3121A>G	NP_001369729.1:p.Thr1041Ala
NM_001382801.1:c.3103A>G	NP_001369730.1:p.Thr1035Ala
NM_001382802.1:c.3049A>G	NP_001369731.1:p.Thr1017Ala
NM_001382803.1:c.3118-247A>G	NP_001369732.1:n.3118-247A>G
NM_001382804.1:c.2479A>G	NP_001369733.1:p.Thr827Ala
NM_001382805.1:c.2356A>G	NP_001369734.1:p.Thr786Ala
NM_001382806.1:c.2269A>G	NP_001369735.1:p.Thr757Ala
NM_004448.4:c.3307A>G MANE Select	NP_004439.2:p.Thr1103Ala
NR_110535.2:n.3545A>G