Canonical Allele Identifier: CA399310674

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143245377
• MyVariant Identifiers: chr17:g.37883665G>T (hg19) ; chr17:g.39727412G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727412G>T , CM000679.2:g.39727412G>T	GRCh38
NC_000017.10:g.37883665G>T , CM000679.1:g.37883665G>T	GRCh37
NC_000017.9:g.35137191G>T	NCBI36
NG_007503.1:g.44273G>T , LRG_724:g.44273G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3277G>T MANE Select	ENSP00000269571.4:p.Gly1093Trp
ENST00000269571.9:c.3277G>T	ENSP00000269571.4:p.Gly1093Trp
ENST00000406381.6:c.3187G>T	ENSP00000385185.2:p.Gly1063Trp
ENST00000445658.6:c.2449G>T	ENSP00000404047.2:p.Gly817Trp
ENST00000541774.5:c.3232G>T	ENSP00000446466.1:p.Gly1078Trp
ENST00000578373.5:c.*3067G>T	ENSP00000463427.1:n.*3067G>T
ENST00000584450.5:c.3160-277G>T	ENSP00000463714.1:n.3160-277G>T
ENST00000584601.5:c.3187G>T	ENSP00000462438.1:p.Gly1063Trp
NM_001005862.2:c.3187G>T , LRG_724t1:c.3187G>T	NP_001005862.1:p.Gly1063Trp
NM_001289936.1:c.3232G>T , LRG_724t4:c.3232G>T	NP_001276865.1:p.Gly1078Trp
NM_001289937.1:c.3160-277G>T	NP_001276866.1:n.3160-277G>T
NM_004448.3:c.3277G>T , LRG_724t2:c.3277G>T	NP_004439.2:p.Gly1093Trp
NR_110535.1:n.3601G>T
XM_024450641.1:c.3415G>T	XP_024306409.1:p.Gly1139Trp
XM_024450642.1:c.3370G>T	XP_024306410.1:p.Gly1124Trp
XM_024450643.1:c.3325G>T	XP_024306411.1:p.Gly1109Trp
NM_001005862.3:c.3187G>T	NP_001005862.1:p.Gly1063Trp
NM_001289936.2:c.3232G>T	NP_001276865.1:p.Gly1078Trp
NM_001289937.2:c.3160-277G>T	NP_001276866.1:n.3160-277G>T
NM_001382782.1:c.3187G>T	NP_001369711.1:p.Gly1063Trp
NM_001382783.1:c.3187G>T	NP_001369712.1:p.Gly1063Trp
NM_001382784.1:c.3394G>T	NP_001369713.1:p.Gly1132Trp
NM_001382785.1:c.3379G>T	NP_001369714.1:p.Gly1127Trp
NM_001382786.1:c.3358G>T	NP_001369715.1:p.Gly1120Trp
NM_001382787.1:c.3352G>T	NP_001369716.1:p.Gly1118Trp
NM_001382788.1:c.3307G>T	NP_001369717.1:p.Gly1103Trp
NM_001382789.1:c.3298G>T	NP_001369718.1:p.Gly1100Trp
NM_001382790.1:c.3274G>T	NP_001369719.1:p.Gly1092Trp
NM_001382791.1:c.3268G>T	NP_001369720.1:p.Gly1090Trp
NM_001382792.1:c.3241G>T	NP_001369721.1:p.Gly1081Trp
NM_001382793.1:c.3235G>T	NP_001369722.1:p.Gly1079Trp
NM_001382794.1:c.3235G>T	NP_001369723.1:p.Gly1079Trp
NM_001382795.1:c.3229G>T	NP_001369724.1:p.Gly1077Trp
NM_001382796.1:c.3190G>T	NP_001369725.1:p.Gly1064Trp
NM_001382797.1:c.3178G>T	NP_001369726.1:p.Gly1060Trp
NM_001382798.1:c.3121G>T	NP_001369727.1:p.Gly1041Trp
NM_001382799.1:c.3097G>T	NP_001369728.1:p.Gly1033Trp
NM_001382800.1:c.3091G>T	NP_001369729.1:p.Gly1031Trp
NM_001382801.1:c.3073G>T	NP_001369730.1:p.Gly1025Trp
NM_001382802.1:c.3019G>T	NP_001369731.1:p.Gly1007Trp
NM_001382803.1:c.3118-277G>T	NP_001369732.1:n.3118-277G>T
NM_001382804.1:c.2449G>T	NP_001369733.1:p.Gly817Trp
NM_001382805.1:c.2326G>T	NP_001369734.1:p.Gly776Trp
NM_001382806.1:c.2239G>T	NP_001369735.1:p.Gly747Trp
NM_004448.4:c.3277G>T MANE Select	NP_004439.2:p.Gly1093Trp
NR_110535.2:n.3515G>T