Canonical Allele Identifier: CA399312703

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37883759C>G (hg19) ; chr17:g.39727506C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727506C>G , CM000679.2:g.39727506C>G	GRCh38
NC_000017.10:g.37883759C>G , CM000679.1:g.37883759C>G	GRCh37
NC_000017.9:g.35137285C>G	NCBI36
NG_007503.1:g.44367C>G , LRG_724:g.44367C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3371C>G MANE Select	ENSP00000269571.4:p.Thr1124Ser
ENST00000269571.9:c.3371C>G	ENSP00000269571.4:p.Thr1124Ser
ENST00000406381.6:c.3281C>G	ENSP00000385185.2:p.Thr1094Ser
ENST00000445658.6:c.2543C>G	ENSP00000404047.2:p.Thr848Ser
ENST00000541774.5:c.3326C>G	ENSP00000446466.1:p.Thr1109Ser
ENST00000578373.5:c.*3161C>G	ENSP00000463427.1:n.*3161C>G
ENST00000584450.5:c.3160-183C>G	ENSP00000463714.1:n.3160-183C>G
ENST00000584601.5:c.3281C>G	ENSP00000462438.1:p.Thr1094Ser
NM_001005862.2:c.3281C>G , LRG_724t1:c.3281C>G	NP_001005862.1:p.Thr1094Ser
NM_001289936.1:c.3326C>G , LRG_724t4:c.3326C>G	NP_001276865.1:p.Thr1109Ser
NM_001289937.1:c.3160-183C>G	NP_001276866.1:n.3160-183C>G
NM_004448.3:c.3371C>G , LRG_724t2:c.3371C>G	NP_004439.2:p.Thr1124Ser
NR_110535.1:n.3695C>G
XM_024450641.1:c.3509C>G	XP_024306409.1:p.Thr1170Ser
XM_024450642.1:c.3464C>G	XP_024306410.1:p.Thr1155Ser
XM_024450643.1:c.3419C>G	XP_024306411.1:p.Thr1140Ser
NM_001005862.3:c.3281C>G	NP_001005862.1:p.Thr1094Ser
NM_001289936.2:c.3326C>G	NP_001276865.1:p.Thr1109Ser
NM_001289937.2:c.3160-183C>G	NP_001276866.1:n.3160-183C>G
NM_001382782.1:c.3281C>G	NP_001369711.1:p.Thr1094Ser
NM_001382783.1:c.3281C>G	NP_001369712.1:p.Thr1094Ser
NM_001382784.1:c.3488C>G	NP_001369713.1:p.Thr1163Ser
NM_001382785.1:c.3473C>G	NP_001369714.1:p.Thr1158Ser
NM_001382786.1:c.3452C>G	NP_001369715.1:p.Thr1151Ser
NM_001382787.1:c.3446C>G	NP_001369716.1:p.Thr1149Ser
NM_001382788.1:c.3401C>G	NP_001369717.1:p.Thr1134Ser
NM_001382789.1:c.3392C>G	NP_001369718.1:p.Thr1131Ser
NM_001382790.1:c.3368C>G	NP_001369719.1:p.Thr1123Ser
NM_001382791.1:c.3362C>G	NP_001369720.1:p.Thr1121Ser
NM_001382792.1:c.3335C>G	NP_001369721.1:p.Thr1112Ser
NM_001382793.1:c.3329C>G	NP_001369722.1:p.Thr1110Ser
NM_001382794.1:c.3329C>G	NP_001369723.1:p.Thr1110Ser
NM_001382795.1:c.3323C>G	NP_001369724.1:p.Thr1108Ser
NM_001382796.1:c.3284C>G	NP_001369725.1:p.Thr1095Ser
NM_001382797.1:c.3272C>G	NP_001369726.1:p.Thr1091Ser
NM_001382798.1:c.3215C>G	NP_001369727.1:p.Thr1072Ser
NM_001382799.1:c.3191C>G	NP_001369728.1:p.Thr1064Ser
NM_001382800.1:c.3185C>G	NP_001369729.1:p.Thr1062Ser
NM_001382801.1:c.3167C>G	NP_001369730.1:p.Thr1056Ser
NM_001382802.1:c.3113C>G	NP_001369731.1:p.Thr1038Ser
NM_001382803.1:c.3118-183C>G	NP_001369732.1:n.3118-183C>G
NM_001382804.1:c.2543C>G	NP_001369733.1:p.Thr848Ser
NM_001382805.1:c.2420C>G	NP_001369734.1:p.Thr807Ser
NM_001382806.1:c.2333C>G	NP_001369735.1:p.Thr778Ser
NM_004448.4:c.3371C>G MANE Select	NP_004439.2:p.Thr1124Ser
NR_110535.2:n.3609C>G