Canonical Allele Identifier: CA399313903

Gene: ERBB2

Linked Data

• dbSNP Id: rs1308088661
• gnomAD v2: 17-37884133-G-A
• gnomAD v4: 17-39727880-G-A
• MyVariant Identifiers: chr17:g.37884133G>A (hg19) ; chr17:g.39727880G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727880G>A , CM000679.2:g.39727880G>A	GRCh38
NC_000017.10:g.37884133G>A , CM000679.1:g.37884133G>A	GRCh37
NC_000017.9:g.35137659G>A	NCBI36
NG_007503.1:g.44741G>A , LRG_724:g.44741G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3604G>A MANE Select	ENSP00000269571.4:p.Gly1202Arg
ENST00000269571.9:c.3604G>A	ENSP00000269571.4:p.Gly1202Arg
ENST00000406381.6:c.3514G>A	ENSP00000385185.2:p.Gly1172Arg
ENST00000445658.6:c.2776G>A	ENSP00000404047.2:p.Gly926Arg
ENST00000541774.5:c.3559G>A	ENSP00000446466.1:p.Gly1187Arg
ENST00000578373.5:c.*3394G>A	ENSP00000463427.1:n.*3394G>A
ENST00000584450.5:c.*183G>A	ENSP00000463714.1:n.*183G>A
ENST00000584601.5:c.3514G>A	ENSP00000462438.1:p.Gly1172Arg
NM_001005862.2:c.3514G>A , LRG_724t1:c.3514G>A	NP_001005862.1:p.Gly1172Arg
NM_001289936.1:c.3559G>A , LRG_724t4:c.3559G>A	NP_001276865.1:p.Gly1187Arg
NM_001289937.1:c.*183G>A	NP_001276866.1:n.*183G>A
NM_004448.3:c.3604G>A , LRG_724t2:c.3604G>A	NP_004439.2:p.Gly1202Arg
NR_110535.1:n.3928G>A
XM_024450641.1:c.3742G>A	XP_024306409.1:p.Gly1248Arg
XM_024450642.1:c.3697G>A	XP_024306410.1:p.Gly1233Arg
XM_024450643.1:c.3652G>A	XP_024306411.1:p.Gly1218Arg
NM_001005862.3:c.3514G>A	NP_001005862.1:p.Gly1172Arg
NM_001289936.2:c.3559G>A	NP_001276865.1:p.Gly1187Arg
NM_001289937.2:c.*183G>A	NP_001276866.1:n.*183G>A
NM_001382782.1:c.3514G>A	NP_001369711.1:p.Gly1172Arg
NM_001382783.1:c.3514G>A	NP_001369712.1:p.Gly1172Arg
NM_001382784.1:c.3721G>A	NP_001369713.1:p.Gly1241Arg
NM_001382785.1:c.3706G>A	NP_001369714.1:p.Gly1236Arg
NM_001382786.1:c.3685G>A	NP_001369715.1:p.Gly1229Arg
NM_001382787.1:c.3679G>A	NP_001369716.1:p.Gly1227Arg
NM_001382788.1:c.3634G>A	NP_001369717.1:p.Gly1212Arg
NM_001382789.1:c.3625G>A	NP_001369718.1:p.Gly1209Arg
NM_001382790.1:c.3601G>A	NP_001369719.1:p.Gly1201Arg
NM_001382791.1:c.3595G>A	NP_001369720.1:p.Gly1199Arg
NM_001382792.1:c.3568G>A	NP_001369721.1:p.Gly1190Arg
NM_001382793.1:c.3562G>A	NP_001369722.1:p.Gly1188Arg
NM_001382794.1:c.3562G>A	NP_001369723.1:p.Gly1188Arg
NM_001382795.1:c.3556G>A	NP_001369724.1:p.Gly1186Arg
NM_001382796.1:c.3517G>A	NP_001369725.1:p.Gly1173Arg
NM_001382797.1:c.3505G>A	NP_001369726.1:p.Gly1169Arg
NM_001382798.1:c.3448G>A	NP_001369727.1:p.Gly1150Arg
NM_001382799.1:c.3424G>A	NP_001369728.1:p.Gly1142Arg
NM_001382800.1:c.3418G>A	NP_001369729.1:p.Gly1140Arg
NM_001382801.1:c.3400G>A	NP_001369730.1:p.Gly1134Arg
NM_001382802.1:c.3346G>A	NP_001369731.1:p.Gly1116Arg
NM_001382803.1:c.*183G>A	NP_001369732.1:n.*183G>A
NM_001382804.1:c.2776G>A	NP_001369733.1:p.Gly926Arg
NM_001382805.1:c.2653G>A	NP_001369734.1:p.Gly885Arg
NM_001382806.1:c.2566G>A	NP_001369735.1:p.Gly856Arg
NM_004448.4:c.3604G>A MANE Select	NP_004439.2:p.Gly1202Arg
NR_110535.2:n.3842G>A