Canonical Allele Identifier: CA399310459

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143240705
• MyVariant Identifiers: chr17:g.37883627G>T (hg19) ; chr17:g.39727374G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727374G>T , CM000679.2:g.39727374G>T	GRCh38
NC_000017.10:g.37883627G>T , CM000679.1:g.37883627G>T	GRCh37
NC_000017.9:g.35137153G>T	NCBI36
NG_007503.1:g.44235G>T , LRG_724:g.44235G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3239G>T MANE Select	ENSP00000269571.4:p.Gly1080Val
ENST00000269571.9:c.3239G>T	ENSP00000269571.4:p.Gly1080Val
ENST00000406381.6:c.3149G>T	ENSP00000385185.2:p.Gly1050Val
ENST00000445658.6:c.2411G>T	ENSP00000404047.2:p.Gly804Val
ENST00000541774.5:c.3194G>T	ENSP00000446466.1:p.Gly1065Val
ENST00000578373.5:c.*3029G>T	ENSP00000463427.1:n.*3029G>T
ENST00000584450.5:c.3160-315G>T	ENSP00000463714.1:n.3160-315G>T
ENST00000584601.5:c.3149G>T	ENSP00000462438.1:p.Gly1050Val
NM_001005862.2:c.3149G>T , LRG_724t1:c.3149G>T	NP_001005862.1:p.Gly1050Val
NM_001289936.1:c.3194G>T , LRG_724t4:c.3194G>T	NP_001276865.1:p.Gly1065Val
NM_001289937.1:c.3160-315G>T	NP_001276866.1:n.3160-315G>T
NM_004448.3:c.3239G>T , LRG_724t2:c.3239G>T	NP_004439.2:p.Gly1080Val
NR_110535.1:n.3563G>T
XM_024450641.1:c.3377G>T	XP_024306409.1:p.Gly1126Val
XM_024450642.1:c.3332G>T	XP_024306410.1:p.Gly1111Val
XM_024450643.1:c.3287G>T	XP_024306411.1:p.Gly1096Val
NM_001005862.3:c.3149G>T	NP_001005862.1:p.Gly1050Val
NM_001289936.2:c.3194G>T	NP_001276865.1:p.Gly1065Val
NM_001289937.2:c.3160-315G>T	NP_001276866.1:n.3160-315G>T
NM_001382782.1:c.3149G>T	NP_001369711.1:p.Gly1050Val
NM_001382783.1:c.3149G>T	NP_001369712.1:p.Gly1050Val
NM_001382784.1:c.3356G>T	NP_001369713.1:p.Gly1119Val
NM_001382785.1:c.3341G>T	NP_001369714.1:p.Gly1114Val
NM_001382786.1:c.3320G>T	NP_001369715.1:p.Gly1107Val
NM_001382787.1:c.3314G>T	NP_001369716.1:p.Gly1105Val
NM_001382788.1:c.3269G>T	NP_001369717.1:p.Gly1090Val
NM_001382789.1:c.3260G>T	NP_001369718.1:p.Gly1087Val
NM_001382790.1:c.3236G>T	NP_001369719.1:p.Gly1079Val
NM_001382791.1:c.3230G>T	NP_001369720.1:p.Gly1077Val
NM_001382792.1:c.3203G>T	NP_001369721.1:p.Gly1068Val
NM_001382793.1:c.3197G>T	NP_001369722.1:p.Gly1066Val
NM_001382794.1:c.3197G>T	NP_001369723.1:p.Gly1066Val
NM_001382795.1:c.3191G>T	NP_001369724.1:p.Gly1064Val
NM_001382796.1:c.3152G>T	NP_001369725.1:p.Gly1051Val
NM_001382797.1:c.3140G>T	NP_001369726.1:p.Gly1047Val
NM_001382798.1:c.3083G>T	NP_001369727.1:p.Gly1028Val
NM_001382799.1:c.3059G>T	NP_001369728.1:p.Gly1020Val
NM_001382800.1:c.3053G>T	NP_001369729.1:p.Gly1018Val
NM_001382801.1:c.3035G>T	NP_001369730.1:p.Gly1012Val
NM_001382802.1:c.2981G>T	NP_001369731.1:p.Gly994Val
NM_001382803.1:c.3118-315G>T	NP_001369732.1:n.3118-315G>T
NM_001382804.1:c.2411G>T	NP_001369733.1:p.Gly804Val
NM_001382805.1:c.2288G>T	NP_001369734.1:p.Gly763Val
NM_001382806.1:c.2201G>T	NP_001369735.1:p.Gly734Val
NM_004448.4:c.3239G>T MANE Select	NP_004439.2:p.Gly1080Val
NR_110535.2:n.3477G>T