Canonical Allele Identifier: CA399312787

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143261126
• MyVariant Identifiers: chr17:g.37883792C>A (hg19) ; chr17:g.39727539C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727539C>A , CM000679.2:g.39727539C>A	GRCh38
NC_000017.10:g.37883792C>A , CM000679.1:g.37883792C>A	GRCh37
NC_000017.9:g.35137318C>A	NCBI36
NG_007503.1:g.44400C>A , LRG_724:g.44400C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3404C>A MANE Select	ENSP00000269571.4:p.Pro1135His
ENST00000269571.9:c.3404C>A	ENSP00000269571.4:p.Pro1135His
ENST00000406381.6:c.3314C>A	ENSP00000385185.2:p.Pro1105His
ENST00000445658.6:c.2576C>A	ENSP00000404047.2:p.Pro859His
ENST00000541774.5:c.3359C>A	ENSP00000446466.1:p.Pro1120His
ENST00000578373.5:c.*3194C>A	ENSP00000463427.1:n.*3194C>A
ENST00000584450.5:c.3160-150C>A	ENSP00000463714.1:n.3160-150C>A
ENST00000584601.5:c.3314C>A	ENSP00000462438.1:p.Pro1105His
NM_001005862.2:c.3314C>A , LRG_724t1:c.3314C>A	NP_001005862.1:p.Pro1105His
NM_001289936.1:c.3359C>A , LRG_724t4:c.3359C>A	NP_001276865.1:p.Pro1120His
NM_001289937.1:c.3160-150C>A	NP_001276866.1:n.3160-150C>A
NM_004448.3:c.3404C>A , LRG_724t2:c.3404C>A	NP_004439.2:p.Pro1135His
NR_110535.1:n.3728C>A
XM_024450641.1:c.3542C>A	XP_024306409.1:p.Pro1181His
XM_024450642.1:c.3497C>A	XP_024306410.1:p.Pro1166His
XM_024450643.1:c.3452C>A	XP_024306411.1:p.Pro1151His
NM_001005862.3:c.3314C>A	NP_001005862.1:p.Pro1105His
NM_001289936.2:c.3359C>A	NP_001276865.1:p.Pro1120His
NM_001289937.2:c.3160-150C>A	NP_001276866.1:n.3160-150C>A
NM_001382782.1:c.3314C>A	NP_001369711.1:p.Pro1105His
NM_001382783.1:c.3314C>A	NP_001369712.1:p.Pro1105His
NM_001382784.1:c.3521C>A	NP_001369713.1:p.Pro1174His
NM_001382785.1:c.3506C>A	NP_001369714.1:p.Pro1169His
NM_001382786.1:c.3485C>A	NP_001369715.1:p.Pro1162His
NM_001382787.1:c.3479C>A	NP_001369716.1:p.Pro1160His
NM_001382788.1:c.3434C>A	NP_001369717.1:p.Pro1145His
NM_001382789.1:c.3425C>A	NP_001369718.1:p.Pro1142His
NM_001382790.1:c.3401C>A	NP_001369719.1:p.Pro1134His
NM_001382791.1:c.3395C>A	NP_001369720.1:p.Pro1132His
NM_001382792.1:c.3368C>A	NP_001369721.1:p.Pro1123His
NM_001382793.1:c.3362C>A	NP_001369722.1:p.Pro1121His
NM_001382794.1:c.3362C>A	NP_001369723.1:p.Pro1121His
NM_001382795.1:c.3356C>A	NP_001369724.1:p.Pro1119His
NM_001382796.1:c.3317C>A	NP_001369725.1:p.Pro1106His
NM_001382797.1:c.3305C>A	NP_001369726.1:p.Pro1102His
NM_001382798.1:c.3248C>A	NP_001369727.1:p.Pro1083His
NM_001382799.1:c.3224C>A	NP_001369728.1:p.Pro1075His
NM_001382800.1:c.3218C>A	NP_001369729.1:p.Pro1073His
NM_001382801.1:c.3200C>A	NP_001369730.1:p.Pro1067His
NM_001382802.1:c.3146C>A	NP_001369731.1:p.Pro1049His
NM_001382803.1:c.3118-150C>A	NP_001369732.1:n.3118-150C>A
NM_001382804.1:c.2576C>A	NP_001369733.1:p.Pro859His
NM_001382805.1:c.2453C>A	NP_001369734.1:p.Pro818His
NM_001382806.1:c.2366C>A	NP_001369735.1:p.Pro789His
NM_004448.4:c.3404C>A MANE Select	NP_004439.2:p.Pro1135His
NR_110535.2:n.3642C>A