Canonical Allele Identifier: CA399312519

Gene: ERBB2

Linked Data

• dbSNP Id: rs1337217429
• MyVariant Identifiers: chr17:g.37883710C>G (hg19) ; chr17:g.39727457C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727457C>G , CM000679.2:g.39727457C>G	GRCh38
NC_000017.10:g.37883710C>G , CM000679.1:g.37883710C>G	GRCh37
NC_000017.9:g.35137236C>G	NCBI36
NG_007503.1:g.44318C>G , LRG_724:g.44318C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3322C>G MANE Select	ENSP00000269571.4:p.Pro1108Ala
ENST00000269571.9:c.3322C>G	ENSP00000269571.4:p.Pro1108Ala
ENST00000406381.6:c.3232C>G	ENSP00000385185.2:p.Pro1078Ala
ENST00000445658.6:c.2494C>G	ENSP00000404047.2:p.Pro832Ala
ENST00000541774.5:c.3277C>G	ENSP00000446466.1:p.Pro1093Ala
ENST00000578373.5:c.*3112C>G	ENSP00000463427.1:n.*3112C>G
ENST00000584450.5:c.3160-232C>G	ENSP00000463714.1:n.3160-232C>G
ENST00000584601.5:c.3232C>G	ENSP00000462438.1:p.Pro1078Ala
NM_001005862.2:c.3232C>G , LRG_724t1:c.3232C>G	NP_001005862.1:p.Pro1078Ala
NM_001289936.1:c.3277C>G , LRG_724t4:c.3277C>G	NP_001276865.1:p.Pro1093Ala
NM_001289937.1:c.3160-232C>G	NP_001276866.1:n.3160-232C>G
NM_004448.3:c.3322C>G , LRG_724t2:c.3322C>G	NP_004439.2:p.Pro1108Ala
NR_110535.1:n.3646C>G
XM_024450641.1:c.3460C>G	XP_024306409.1:p.Pro1154Ala
XM_024450642.1:c.3415C>G	XP_024306410.1:p.Pro1139Ala
XM_024450643.1:c.3370C>G	XP_024306411.1:p.Pro1124Ala
NM_001005862.3:c.3232C>G	NP_001005862.1:p.Pro1078Ala
NM_001289936.2:c.3277C>G	NP_001276865.1:p.Pro1093Ala
NM_001289937.2:c.3160-232C>G	NP_001276866.1:n.3160-232C>G
NM_001382782.1:c.3232C>G	NP_001369711.1:p.Pro1078Ala
NM_001382783.1:c.3232C>G	NP_001369712.1:p.Pro1078Ala
NM_001382784.1:c.3439C>G	NP_001369713.1:p.Pro1147Ala
NM_001382785.1:c.3424C>G	NP_001369714.1:p.Pro1142Ala
NM_001382786.1:c.3403C>G	NP_001369715.1:p.Pro1135Ala
NM_001382787.1:c.3397C>G	NP_001369716.1:p.Pro1133Ala
NM_001382788.1:c.3352C>G	NP_001369717.1:p.Pro1118Ala
NM_001382789.1:c.3343C>G	NP_001369718.1:p.Pro1115Ala
NM_001382790.1:c.3319C>G	NP_001369719.1:p.Pro1107Ala
NM_001382791.1:c.3313C>G	NP_001369720.1:p.Pro1105Ala
NM_001382792.1:c.3286C>G	NP_001369721.1:p.Pro1096Ala
NM_001382793.1:c.3280C>G	NP_001369722.1:p.Pro1094Ala
NM_001382794.1:c.3280C>G	NP_001369723.1:p.Pro1094Ala
NM_001382795.1:c.3274C>G	NP_001369724.1:p.Pro1092Ala
NM_001382796.1:c.3235C>G	NP_001369725.1:p.Pro1079Ala
NM_001382797.1:c.3223C>G	NP_001369726.1:p.Pro1075Ala
NM_001382798.1:c.3166C>G	NP_001369727.1:p.Pro1056Ala
NM_001382799.1:c.3142C>G	NP_001369728.1:p.Pro1048Ala
NM_001382800.1:c.3136C>G	NP_001369729.1:p.Pro1046Ala
NM_001382801.1:c.3118C>G	NP_001369730.1:p.Pro1040Ala
NM_001382802.1:c.3064C>G	NP_001369731.1:p.Pro1022Ala
NM_001382803.1:c.3118-232C>G	NP_001369732.1:n.3118-232C>G
NM_001382804.1:c.2494C>G	NP_001369733.1:p.Pro832Ala
NM_001382805.1:c.2371C>G	NP_001369734.1:p.Pro791Ala
NM_001382806.1:c.2284C>G	NP_001369735.1:p.Pro762Ala
NM_004448.4:c.3322C>G MANE Select	NP_004439.2:p.Pro1108Ala
NR_110535.2:n.3560C>G