Canonical Allele Identifier: CA399310217

Gene: ERBB2

Linked Data

• dbSNP Id: rs997168711
• MyVariant Identifiers: chr17:g.37883581C>A (hg19) ; chr17:g.39727328C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727328C>A , CM000679.2:g.39727328C>A	GRCh38
NC_000017.10:g.37883581C>A , CM000679.1:g.37883581C>A	GRCh37
NC_000017.9:g.35137107C>A	NCBI36
NG_007503.1:g.44189C>A , LRG_724:g.44189C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3193C>A MANE Select	ENSP00000269571.4:p.Pro1065Thr
ENST00000269571.9:c.3193C>A	ENSP00000269571.4:p.Pro1065Thr
ENST00000406381.6:c.3103C>A	ENSP00000385185.2:p.Pro1035Thr
ENST00000445658.6:c.2365C>A	ENSP00000404047.2:p.Pro789Thr
ENST00000541774.5:c.3148C>A	ENSP00000446466.1:p.Pro1050Thr
ENST00000578373.5:c.*2983C>A	ENSP00000463427.1:n.*2983C>A
ENST00000584450.5:c.3159+325C>A	ENSP00000463714.1:n.3159+325C>A
ENST00000584601.5:c.3103C>A	ENSP00000462438.1:p.Pro1035Thr
NM_001005862.2:c.3103C>A , LRG_724t1:c.3103C>A	NP_001005862.1:p.Pro1035Thr
NM_001289936.1:c.3148C>A , LRG_724t4:c.3148C>A	NP_001276865.1:p.Pro1050Thr
NM_001289937.1:c.3159+325C>A	NP_001276866.1:n.3159+325C>A
NM_004448.3:c.3193C>A , LRG_724t2:c.3193C>A	NP_004439.2:p.Pro1065Thr
NR_110535.1:n.3517C>A
XM_024450641.1:c.3331C>A	XP_024306409.1:p.Pro1111Thr
XM_024450642.1:c.3286C>A	XP_024306410.1:p.Pro1096Thr
XM_024450643.1:c.3241C>A	XP_024306411.1:p.Pro1081Thr
NM_001005862.3:c.3103C>A	NP_001005862.1:p.Pro1035Thr
NM_001289936.2:c.3148C>A	NP_001276865.1:p.Pro1050Thr
NM_001289937.2:c.3159+325C>A	NP_001276866.1:n.3159+325C>A
NM_001382782.1:c.3103C>A	NP_001369711.1:p.Pro1035Thr
NM_001382783.1:c.3103C>A	NP_001369712.1:p.Pro1035Thr
NM_001382784.1:c.3310C>A	NP_001369713.1:p.Pro1104Thr
NM_001382785.1:c.3295C>A	NP_001369714.1:p.Pro1099Thr
NM_001382786.1:c.3274C>A	NP_001369715.1:p.Pro1092Thr
NM_001382787.1:c.3268C>A	NP_001369716.1:p.Pro1090Thr
NM_001382788.1:c.3223C>A	NP_001369717.1:p.Pro1075Thr
NM_001382789.1:c.3214C>A	NP_001369718.1:p.Pro1072Thr
NM_001382790.1:c.3190C>A	NP_001369719.1:p.Pro1064Thr
NM_001382791.1:c.3184C>A	NP_001369720.1:p.Pro1062Thr
NM_001382792.1:c.3157C>A	NP_001369721.1:p.Pro1053Thr
NM_001382793.1:c.3151C>A	NP_001369722.1:p.Pro1051Thr
NM_001382794.1:c.3151C>A	NP_001369723.1:p.Pro1051Thr
NM_001382795.1:c.3145C>A	NP_001369724.1:p.Pro1049Thr
NM_001382796.1:c.3106C>A	NP_001369725.1:p.Pro1036Thr
NM_001382797.1:c.3094C>A	NP_001369726.1:p.Pro1032Thr
NM_001382798.1:c.3037C>A	NP_001369727.1:p.Pro1013Thr
NM_001382799.1:c.3013C>A	NP_001369728.1:p.Pro1005Thr
NM_001382800.1:c.3007C>A	NP_001369729.1:p.Pro1003Thr
NM_001382801.1:c.2989C>A	NP_001369730.1:p.Pro997Thr
NM_001382802.1:c.2935C>A	NP_001369731.1:p.Pro979Thr
NM_001382803.1:c.3117+325C>A	NP_001369732.1:n.3117+325C>A
NM_001382804.1:c.2365C>A	NP_001369733.1:p.Pro789Thr
NM_001382805.1:c.2242C>A	NP_001369734.1:p.Pro748Thr
NM_001382806.1:c.2155C>A	NP_001369735.1:p.Pro719Thr
NM_004448.4:c.3193C>A MANE Select	NP_004439.2:p.Pro1065Thr
NR_110535.2:n.3431C>A