Canonical Allele Identifier: CA399310220
Gene: ERBB2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39727329C>G , CM000679.2:g.39727329C>G GRCh38
NC_000017.10:g.37883582C>G , CM000679.1:g.37883582C>G GRCh37
NC_000017.9:g.35137108C>G NCBI36
NG_007503.1:g.44190C>G , LRG_724:g.44190C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000269571.10:c.3194C>G MANE Select ENSP00000269571.4:p.Pro1065Arg
ENST00000269571.9:c.3194C>G ENSP00000269571.4:p.Pro1065Arg
ENST00000406381.6:c.3104C>G ENSP00000385185.2:p.Pro1035Arg
ENST00000445658.6:c.2366C>G ENSP00000404047.2:p.Pro789Arg
ENST00000541774.5:c.3149C>G ENSP00000446466.1:p.Pro1050Arg
ENST00000578373.5:c.*2984C>G ENSP00000463427.1:n.*2984C>G
ENST00000584450.5:c.3159+326C>G ENSP00000463714.1:n.3159+326C>G
ENST00000584601.5:c.3104C>G ENSP00000462438.1:p.Pro1035Arg
NM_001005862.2:c.3104C>G , LRG_724t1:c.3104C>G NP_001005862.1:p.Pro1035Arg
NM_001289936.1:c.3149C>G , LRG_724t4:c.3149C>G NP_001276865.1:p.Pro1050Arg
NM_001289937.1:c.3159+326C>G NP_001276866.1:n.3159+326C>G
NM_004448.3:c.3194C>G , LRG_724t2:c.3194C>G NP_004439.2:p.Pro1065Arg
NR_110535.1:n.3518C>G
XM_024450641.1:c.3332C>G XP_024306409.1:p.Pro1111Arg
XM_024450642.1:c.3287C>G XP_024306410.1:p.Pro1096Arg
XM_024450643.1:c.3242C>G XP_024306411.1:p.Pro1081Arg
NM_001005862.3:c.3104C>G NP_001005862.1:p.Pro1035Arg
NM_001289936.2:c.3149C>G NP_001276865.1:p.Pro1050Arg
NM_001289937.2:c.3159+326C>G NP_001276866.1:n.3159+326C>G
NM_001382782.1:c.3104C>G NP_001369711.1:p.Pro1035Arg
NM_001382783.1:c.3104C>G NP_001369712.1:p.Pro1035Arg
NM_001382784.1:c.3311C>G NP_001369713.1:p.Pro1104Arg
NM_001382785.1:c.3296C>G NP_001369714.1:p.Pro1099Arg
NM_001382786.1:c.3275C>G NP_001369715.1:p.Pro1092Arg
NM_001382787.1:c.3269C>G NP_001369716.1:p.Pro1090Arg
NM_001382788.1:c.3224C>G NP_001369717.1:p.Pro1075Arg
NM_001382789.1:c.3215C>G NP_001369718.1:p.Pro1072Arg
NM_001382790.1:c.3191C>G NP_001369719.1:p.Pro1064Arg
NM_001382791.1:c.3185C>G NP_001369720.1:p.Pro1062Arg
NM_001382792.1:c.3158C>G NP_001369721.1:p.Pro1053Arg
NM_001382793.1:c.3152C>G NP_001369722.1:p.Pro1051Arg
NM_001382794.1:c.3152C>G NP_001369723.1:p.Pro1051Arg
NM_001382795.1:c.3146C>G NP_001369724.1:p.Pro1049Arg
NM_001382796.1:c.3107C>G NP_001369725.1:p.Pro1036Arg
NM_001382797.1:c.3095C>G NP_001369726.1:p.Pro1032Arg
NM_001382798.1:c.3038C>G NP_001369727.1:p.Pro1013Arg
NM_001382799.1:c.3014C>G NP_001369728.1:p.Pro1005Arg
NM_001382800.1:c.3008C>G NP_001369729.1:p.Pro1003Arg
NM_001382801.1:c.2990C>G NP_001369730.1:p.Pro997Arg
NM_001382802.1:c.2936C>G NP_001369731.1:p.Pro979Arg
NM_001382803.1:c.3117+326C>G NP_001369732.1:n.3117+326C>G
NM_001382804.1:c.2366C>G NP_001369733.1:p.Pro789Arg
NM_001382805.1:c.2243C>G NP_001369734.1:p.Pro748Arg
NM_001382806.1:c.2156C>G NP_001369735.1:p.Pro719Arg
NM_004448.4:c.3194C>G MANE Select NP_004439.2:p.Pro1065Arg
NR_110535.2:n.3432C>G