Canonical Allele Identifier: CA399310302

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143237359
• MyVariant Identifiers: chr17:g.37883600C>G (hg19) ; chr17:g.39727347C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727347C>G , CM000679.2:g.39727347C>G	GRCh38
NC_000017.10:g.37883600C>G , CM000679.1:g.37883600C>G	GRCh37
NC_000017.9:g.35137126C>G	NCBI36
NG_007503.1:g.44208C>G , LRG_724:g.44208C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3212C>G MANE Select	ENSP00000269571.4:p.Pro1071Arg
ENST00000269571.9:c.3212C>G	ENSP00000269571.4:p.Pro1071Arg
ENST00000406381.6:c.3122C>G	ENSP00000385185.2:p.Pro1041Arg
ENST00000445658.6:c.2384C>G	ENSP00000404047.2:p.Pro795Arg
ENST00000541774.5:c.3167C>G	ENSP00000446466.1:p.Pro1056Arg
ENST00000578373.5:c.*3002C>G	ENSP00000463427.1:n.*3002C>G
ENST00000584450.5:c.3160-342C>G	ENSP00000463714.1:n.3160-342C>G
ENST00000584601.5:c.3122C>G	ENSP00000462438.1:p.Pro1041Arg
NM_001005862.2:c.3122C>G , LRG_724t1:c.3122C>G	NP_001005862.1:p.Pro1041Arg
NM_001289936.1:c.3167C>G , LRG_724t4:c.3167C>G	NP_001276865.1:p.Pro1056Arg
NM_001289937.1:c.3160-342C>G	NP_001276866.1:n.3160-342C>G
NM_004448.3:c.3212C>G , LRG_724t2:c.3212C>G	NP_004439.2:p.Pro1071Arg
NR_110535.1:n.3536C>G
XM_024450641.1:c.3350C>G	XP_024306409.1:p.Pro1117Arg
XM_024450642.1:c.3305C>G	XP_024306410.1:p.Pro1102Arg
XM_024450643.1:c.3260C>G	XP_024306411.1:p.Pro1087Arg
NM_001005862.3:c.3122C>G	NP_001005862.1:p.Pro1041Arg
NM_001289936.2:c.3167C>G	NP_001276865.1:p.Pro1056Arg
NM_001289937.2:c.3160-342C>G	NP_001276866.1:n.3160-342C>G
NM_001382782.1:c.3122C>G	NP_001369711.1:p.Pro1041Arg
NM_001382783.1:c.3122C>G	NP_001369712.1:p.Pro1041Arg
NM_001382784.1:c.3329C>G	NP_001369713.1:p.Pro1110Arg
NM_001382785.1:c.3314C>G	NP_001369714.1:p.Pro1105Arg
NM_001382786.1:c.3293C>G	NP_001369715.1:p.Pro1098Arg
NM_001382787.1:c.3287C>G	NP_001369716.1:p.Pro1096Arg
NM_001382788.1:c.3242C>G	NP_001369717.1:p.Pro1081Arg
NM_001382789.1:c.3233C>G	NP_001369718.1:p.Pro1078Arg
NM_001382790.1:c.3209C>G	NP_001369719.1:p.Pro1070Arg
NM_001382791.1:c.3203C>G	NP_001369720.1:p.Pro1068Arg
NM_001382792.1:c.3176C>G	NP_001369721.1:p.Pro1059Arg
NM_001382793.1:c.3170C>G	NP_001369722.1:p.Pro1057Arg
NM_001382794.1:c.3170C>G	NP_001369723.1:p.Pro1057Arg
NM_001382795.1:c.3164C>G	NP_001369724.1:p.Pro1055Arg
NM_001382796.1:c.3125C>G	NP_001369725.1:p.Pro1042Arg
NM_001382797.1:c.3113C>G	NP_001369726.1:p.Pro1038Arg
NM_001382798.1:c.3056C>G	NP_001369727.1:p.Pro1019Arg
NM_001382799.1:c.3032C>G	NP_001369728.1:p.Pro1011Arg
NM_001382800.1:c.3026C>G	NP_001369729.1:p.Pro1009Arg
NM_001382801.1:c.3008C>G	NP_001369730.1:p.Pro1003Arg
NM_001382802.1:c.2954C>G	NP_001369731.1:p.Pro985Arg
NM_001382803.1:c.3118-342C>G	NP_001369732.1:n.3118-342C>G
NM_001382804.1:c.2384C>G	NP_001369733.1:p.Pro795Arg
NM_001382805.1:c.2261C>G	NP_001369734.1:p.Pro754Arg
NM_001382806.1:c.2174C>G	NP_001369735.1:p.Pro725Arg
NM_004448.4:c.3212C>G MANE Select	NP_004439.2:p.Pro1071Arg
NR_110535.2:n.3450C>G