Canonical Allele Identifier: CA399313953

Gene: ERBB2

Linked Data

• dbSNP Id: rs373605104
• MyVariant Identifiers: chr17:g.37884140C>A (hg19) ; chr17:g.39727887C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727887C>A , CM000679.2:g.39727887C>A	GRCh38
NC_000017.10:g.37884140C>A , CM000679.1:g.37884140C>A	GRCh37
NC_000017.9:g.35137666C>A	NCBI36
NG_007503.1:g.44748C>A , LRG_724:g.44748C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3611C>A MANE Select	ENSP00000269571.4:p.Ala1204Asp
ENST00000269571.9:c.3611C>A	ENSP00000269571.4:p.Ala1204Asp
ENST00000406381.6:c.3521C>A	ENSP00000385185.2:p.Ala1174Asp
ENST00000445658.6:c.2783C>A	ENSP00000404047.2:p.Ala928Asp
ENST00000541774.5:c.3566C>A	ENSP00000446466.1:p.Ala1189Asp
ENST00000578373.5:c.*3401C>A	ENSP00000463427.1:n.*3401C>A
ENST00000584450.5:c.*190C>A	ENSP00000463714.1:n.*190C>A
ENST00000584601.5:c.3521C>A	ENSP00000462438.1:p.Ala1174Asp
NM_001005862.2:c.3521C>A , LRG_724t1:c.3521C>A	NP_001005862.1:p.Ala1174Asp
NM_001289936.1:c.3566C>A , LRG_724t4:c.3566C>A	NP_001276865.1:p.Ala1189Asp
NM_001289937.1:c.*190C>A	NP_001276866.1:n.*190C>A
NM_004448.3:c.3611C>A , LRG_724t2:c.3611C>A	NP_004439.2:p.Ala1204Asp
NR_110535.1:n.3935C>A
XM_024450641.1:c.3749C>A	XP_024306409.1:p.Ala1250Asp
XM_024450642.1:c.3704C>A	XP_024306410.1:p.Ala1235Asp
XM_024450643.1:c.3659C>A	XP_024306411.1:p.Ala1220Asp
NM_001005862.3:c.3521C>A	NP_001005862.1:p.Ala1174Asp
NM_001289936.2:c.3566C>A	NP_001276865.1:p.Ala1189Asp
NM_001289937.2:c.*190C>A	NP_001276866.1:n.*190C>A
NM_001382782.1:c.3521C>A	NP_001369711.1:p.Ala1174Asp
NM_001382783.1:c.3521C>A	NP_001369712.1:p.Ala1174Asp
NM_001382784.1:c.3728C>A	NP_001369713.1:p.Ala1243Asp
NM_001382785.1:c.3713C>A	NP_001369714.1:p.Ala1238Asp
NM_001382786.1:c.3692C>A	NP_001369715.1:p.Ala1231Asp
NM_001382787.1:c.3686C>A	NP_001369716.1:p.Ala1229Asp
NM_001382788.1:c.3641C>A	NP_001369717.1:p.Ala1214Asp
NM_001382789.1:c.3632C>A	NP_001369718.1:p.Ala1211Asp
NM_001382790.1:c.3608C>A	NP_001369719.1:p.Ala1203Asp
NM_001382791.1:c.3602C>A	NP_001369720.1:p.Ala1201Asp
NM_001382792.1:c.3575C>A	NP_001369721.1:p.Ala1192Asp
NM_001382793.1:c.3569C>A	NP_001369722.1:p.Ala1190Asp
NM_001382794.1:c.3569C>A	NP_001369723.1:p.Ala1190Asp
NM_001382795.1:c.3563C>A	NP_001369724.1:p.Ala1188Asp
NM_001382796.1:c.3524C>A	NP_001369725.1:p.Ala1175Asp
NM_001382797.1:c.3512C>A	NP_001369726.1:p.Ala1171Asp
NM_001382798.1:c.3455C>A	NP_001369727.1:p.Ala1152Asp
NM_001382799.1:c.3431C>A	NP_001369728.1:p.Ala1144Asp
NM_001382800.1:c.3425C>A	NP_001369729.1:p.Ala1142Asp
NM_001382801.1:c.3407C>A	NP_001369730.1:p.Ala1136Asp
NM_001382802.1:c.3353C>A	NP_001369731.1:p.Ala1118Asp
NM_001382803.1:c.*190C>A	NP_001369732.1:n.*190C>A
NM_001382804.1:c.2783C>A	NP_001369733.1:p.Ala928Asp
NM_001382805.1:c.2660C>A	NP_001369734.1:p.Ala887Asp
NM_001382806.1:c.2573C>A	NP_001369735.1:p.Ala858Asp
NM_004448.4:c.3611C>A MANE Select	NP_004439.2:p.Ala1204Asp
NR_110535.2:n.3849C>A