Canonical Allele Identifier: CA399310811

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143247797
• MyVariant Identifiers: chr17:g.37883684A>C (hg19) ; chr17:g.39727431A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727431A>C , CM000679.2:g.39727431A>C	GRCh38
NC_000017.10:g.37883684A>C , CM000679.1:g.37883684A>C	GRCh37
NC_000017.9:g.35137210A>C	NCBI36
NG_007503.1:g.44292A>C , LRG_724:g.44292A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3296A>C MANE Select	ENSP00000269571.4:p.Gln1099Pro
ENST00000269571.9:c.3296A>C	ENSP00000269571.4:p.Gln1099Pro
ENST00000406381.6:c.3206A>C	ENSP00000385185.2:p.Gln1069Pro
ENST00000445658.6:c.2468A>C	ENSP00000404047.2:p.Gln823Pro
ENST00000541774.5:c.3251A>C	ENSP00000446466.1:p.Gln1084Pro
ENST00000578373.5:c.*3086A>C	ENSP00000463427.1:n.*3086A>C
ENST00000584450.5:c.3160-258A>C	ENSP00000463714.1:n.3160-258A>C
ENST00000584601.5:c.3206A>C	ENSP00000462438.1:p.Gln1069Pro
NM_001005862.2:c.3206A>C , LRG_724t1:c.3206A>C	NP_001005862.1:p.Gln1069Pro
NM_001289936.1:c.3251A>C , LRG_724t4:c.3251A>C	NP_001276865.1:p.Gln1084Pro
NM_001289937.1:c.3160-258A>C	NP_001276866.1:n.3160-258A>C
NM_004448.3:c.3296A>C , LRG_724t2:c.3296A>C	NP_004439.2:p.Gln1099Pro
NR_110535.1:n.3620A>C
XM_024450641.1:c.3434A>C	XP_024306409.1:p.Gln1145Pro
XM_024450642.1:c.3389A>C	XP_024306410.1:p.Gln1130Pro
XM_024450643.1:c.3344A>C	XP_024306411.1:p.Gln1115Pro
NM_001005862.3:c.3206A>C	NP_001005862.1:p.Gln1069Pro
NM_001289936.2:c.3251A>C	NP_001276865.1:p.Gln1084Pro
NM_001289937.2:c.3160-258A>C	NP_001276866.1:n.3160-258A>C
NM_001382782.1:c.3206A>C	NP_001369711.1:p.Gln1069Pro
NM_001382783.1:c.3206A>C	NP_001369712.1:p.Gln1069Pro
NM_001382784.1:c.3413A>C	NP_001369713.1:p.Gln1138Pro
NM_001382785.1:c.3398A>C	NP_001369714.1:p.Gln1133Pro
NM_001382786.1:c.3377A>C	NP_001369715.1:p.Gln1126Pro
NM_001382787.1:c.3371A>C	NP_001369716.1:p.Gln1124Pro
NM_001382788.1:c.3326A>C	NP_001369717.1:p.Gln1109Pro
NM_001382789.1:c.3317A>C	NP_001369718.1:p.Gln1106Pro
NM_001382790.1:c.3293A>C	NP_001369719.1:p.Gln1098Pro
NM_001382791.1:c.3287A>C	NP_001369720.1:p.Gln1096Pro
NM_001382792.1:c.3260A>C	NP_001369721.1:p.Gln1087Pro
NM_001382793.1:c.3254A>C	NP_001369722.1:p.Gln1085Pro
NM_001382794.1:c.3254A>C	NP_001369723.1:p.Gln1085Pro
NM_001382795.1:c.3248A>C	NP_001369724.1:p.Gln1083Pro
NM_001382796.1:c.3209A>C	NP_001369725.1:p.Gln1070Pro
NM_001382797.1:c.3197A>C	NP_001369726.1:p.Gln1066Pro
NM_001382798.1:c.3140A>C	NP_001369727.1:p.Gln1047Pro
NM_001382799.1:c.3116A>C	NP_001369728.1:p.Gln1039Pro
NM_001382800.1:c.3110A>C	NP_001369729.1:p.Gln1037Pro
NM_001382801.1:c.3092A>C	NP_001369730.1:p.Gln1031Pro
NM_001382802.1:c.3038A>C	NP_001369731.1:p.Gln1013Pro
NM_001382803.1:c.3118-258A>C	NP_001369732.1:n.3118-258A>C
NM_001382804.1:c.2468A>C	NP_001369733.1:p.Gln823Pro
NM_001382805.1:c.2345A>C	NP_001369734.1:p.Gln782Pro
NM_001382806.1:c.2258A>C	NP_001369735.1:p.Gln753Pro
NM_004448.4:c.3296A>C MANE Select	NP_004439.2:p.Gln1099Pro
NR_110535.2:n.3534A>C