Canonical Allele Identifier: CA399313907

Gene: ERBB2

Linked Data

• dbSNP Id: rs1308088661
• MyVariant Identifiers: chr17:g.37884133G>T (hg19) ; chr17:g.39727880G>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3604G>T MANE Select	ENSP00000269571.4:p.Gly1202Ter
ENST00000269571.9:c.3604G>T	ENSP00000269571.4:p.Gly1202Ter
ENST00000406381.6:c.3514G>T	ENSP00000385185.2:p.Gly1172Ter
ENST00000445658.6:c.2776G>T	ENSP00000404047.2:p.Gly926Ter
ENST00000541774.5:c.3559G>T	ENSP00000446466.1:p.Gly1187Ter
ENST00000578373.5:c.*3394G>T	ENSP00000463427.1:n.*3394G>T
ENST00000584450.5:c.*183G>T	ENSP00000463714.1:n.*183G>T
ENST00000584601.5:c.3514G>T	ENSP00000462438.1:p.Gly1172Ter
NM_001005862.2:c.3514G>T , LRG_724t1:c.3514G>T	NP_001005862.1:p.Gly1172Ter
NM_001289936.1:c.3559G>T , LRG_724t4:c.3559G>T	NP_001276865.1:p.Gly1187Ter
NM_001289937.1:c.*183G>T	NP_001276866.1:n.*183G>T
NM_004448.3:c.3604G>T , LRG_724t2:c.3604G>T	NP_004439.2:p.Gly1202Ter
NR_110535.1:n.3928G>T
XM_024450641.1:c.3742G>T	XP_024306409.1:p.Gly1248Ter
XM_024450642.1:c.3697G>T	XP_024306410.1:p.Gly1233Ter
XM_024450643.1:c.3652G>T	XP_024306411.1:p.Gly1218Ter
NM_001005862.3:c.3514G>T	NP_001005862.1:p.Gly1172Ter
NM_001289936.2:c.3559G>T	NP_001276865.1:p.Gly1187Ter
NM_001289937.2:c.*183G>T	NP_001276866.1:n.*183G>T
NM_001382782.1:c.3514G>T	NP_001369711.1:p.Gly1172Ter
NM_001382783.1:c.3514G>T	NP_001369712.1:p.Gly1172Ter
NM_001382784.1:c.3721G>T	NP_001369713.1:p.Gly1241Ter
NM_001382785.1:c.3706G>T	NP_001369714.1:p.Gly1236Ter
NM_001382786.1:c.3685G>T	NP_001369715.1:p.Gly1229Ter
NM_001382787.1:c.3679G>T	NP_001369716.1:p.Gly1227Ter
NM_001382788.1:c.3634G>T	NP_001369717.1:p.Gly1212Ter
NM_001382789.1:c.3625G>T	NP_001369718.1:p.Gly1209Ter
NM_001382790.1:c.3601G>T	NP_001369719.1:p.Gly1201Ter
NM_001382791.1:c.3595G>T	NP_001369720.1:p.Gly1199Ter
NM_001382792.1:c.3568G>T	NP_001369721.1:p.Gly1190Ter
NM_001382793.1:c.3562G>T	NP_001369722.1:p.Gly1188Ter
NM_001382794.1:c.3562G>T	NP_001369723.1:p.Gly1188Ter
NM_001382795.1:c.3556G>T	NP_001369724.1:p.Gly1186Ter
NM_001382796.1:c.3517G>T	NP_001369725.1:p.Gly1173Ter
NM_001382797.1:c.3505G>T	NP_001369726.1:p.Gly1169Ter
NM_001382798.1:c.3448G>T	NP_001369727.1:p.Gly1150Ter
NM_001382799.1:c.3424G>T	NP_001369728.1:p.Gly1142Ter
NM_001382800.1:c.3418G>T	NP_001369729.1:p.Gly1140Ter
NM_001382801.1:c.3400G>T	NP_001369730.1:p.Gly1134Ter
NM_001382802.1:c.3346G>T	NP_001369731.1:p.Gly1116Ter
NM_001382803.1:c.*183G>T	NP_001369732.1:n.*183G>T
NM_001382804.1:c.2776G>T	NP_001369733.1:p.Gly926Ter
NM_001382805.1:c.2653G>T	NP_001369734.1:p.Gly885Ter
NM_001382806.1:c.2566G>T	NP_001369735.1:p.Gly856Ter
NM_004448.4:c.3604G>T MANE Select	NP_004439.2:p.Gly1202Ter
NR_110535.2:n.3842G>T