Canonical Allele Identifier: CA399310839

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143248046
• MyVariant Identifiers: chr17:g.37883686A>C (hg19) ; chr17:g.39727433A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727433A>C , CM000679.2:g.39727433A>C	GRCh38
NC_000017.10:g.37883686A>C , CM000679.1:g.37883686A>C	GRCh37
NC_000017.9:g.35137212A>C	NCBI36
NG_007503.1:g.44294A>C , LRG_724:g.44294A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3298A>C MANE Select	ENSP00000269571.4:p.Ser1100Arg
ENST00000269571.9:c.3298A>C	ENSP00000269571.4:p.Ser1100Arg
ENST00000406381.6:c.3208A>C	ENSP00000385185.2:p.Ser1070Arg
ENST00000445658.6:c.2470A>C	ENSP00000404047.2:p.Ser824Arg
ENST00000541774.5:c.3253A>C	ENSP00000446466.1:p.Ser1085Arg
ENST00000578373.5:c.*3088A>C	ENSP00000463427.1:n.*3088A>C
ENST00000584450.5:c.3160-256A>C	ENSP00000463714.1:n.3160-256A>C
ENST00000584601.5:c.3208A>C	ENSP00000462438.1:p.Ser1070Arg
NM_001005862.2:c.3208A>C , LRG_724t1:c.3208A>C	NP_001005862.1:p.Ser1070Arg
NM_001289936.1:c.3253A>C , LRG_724t4:c.3253A>C	NP_001276865.1:p.Ser1085Arg
NM_001289937.1:c.3160-256A>C	NP_001276866.1:n.3160-256A>C
NM_004448.3:c.3298A>C , LRG_724t2:c.3298A>C	NP_004439.2:p.Ser1100Arg
NR_110535.1:n.3622A>C
XM_024450641.1:c.3436A>C	XP_024306409.1:p.Ser1146Arg
XM_024450642.1:c.3391A>C	XP_024306410.1:p.Ser1131Arg
XM_024450643.1:c.3346A>C	XP_024306411.1:p.Ser1116Arg
NM_001005862.3:c.3208A>C	NP_001005862.1:p.Ser1070Arg
NM_001289936.2:c.3253A>C	NP_001276865.1:p.Ser1085Arg
NM_001289937.2:c.3160-256A>C	NP_001276866.1:n.3160-256A>C
NM_001382782.1:c.3208A>C	NP_001369711.1:p.Ser1070Arg
NM_001382783.1:c.3208A>C	NP_001369712.1:p.Ser1070Arg
NM_001382784.1:c.3415A>C	NP_001369713.1:p.Ser1139Arg
NM_001382785.1:c.3400A>C	NP_001369714.1:p.Ser1134Arg
NM_001382786.1:c.3379A>C	NP_001369715.1:p.Ser1127Arg
NM_001382787.1:c.3373A>C	NP_001369716.1:p.Ser1125Arg
NM_001382788.1:c.3328A>C	NP_001369717.1:p.Ser1110Arg
NM_001382789.1:c.3319A>C	NP_001369718.1:p.Ser1107Arg
NM_001382790.1:c.3295A>C	NP_001369719.1:p.Ser1099Arg
NM_001382791.1:c.3289A>C	NP_001369720.1:p.Ser1097Arg
NM_001382792.1:c.3262A>C	NP_001369721.1:p.Ser1088Arg
NM_001382793.1:c.3256A>C	NP_001369722.1:p.Ser1086Arg
NM_001382794.1:c.3256A>C	NP_001369723.1:p.Ser1086Arg
NM_001382795.1:c.3250A>C	NP_001369724.1:p.Ser1084Arg
NM_001382796.1:c.3211A>C	NP_001369725.1:p.Ser1071Arg
NM_001382797.1:c.3199A>C	NP_001369726.1:p.Ser1067Arg
NM_001382798.1:c.3142A>C	NP_001369727.1:p.Ser1048Arg
NM_001382799.1:c.3118A>C	NP_001369728.1:p.Ser1040Arg
NM_001382800.1:c.3112A>C	NP_001369729.1:p.Ser1038Arg
NM_001382801.1:c.3094A>C	NP_001369730.1:p.Ser1032Arg
NM_001382802.1:c.3040A>C	NP_001369731.1:p.Ser1014Arg
NM_001382803.1:c.3118-256A>C	NP_001369732.1:n.3118-256A>C
NM_001382804.1:c.2470A>C	NP_001369733.1:p.Ser824Arg
NM_001382805.1:c.2347A>C	NP_001369734.1:p.Ser783Arg
NM_001382806.1:c.2260A>C	NP_001369735.1:p.Ser754Arg
NM_004448.4:c.3298A>C MANE Select	NP_004439.2:p.Ser1100Arg
NR_110535.2:n.3536A>C