Canonical Allele Identifier: CA499890815

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143308998
• MyVariant Identifiers: chr17:g.37884150C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727897C>G , CM000679.2:g.39727897C>G	GRCh38
NC_000017.10:g.37884150C>G , CM000679.1:g.37884150C>G	GRCh37
NC_000017.9:g.35137676C>G	NCBI36
NG_007503.1:g.44758C>G , LRG_724:g.44758C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3621C>G MANE Select	ENSP00000269571.4:p.Pro1207=
ENST00000269571.9:c.3621C>G	ENSP00000269571.4:p.Pro1207=
ENST00000406381.6:c.3531C>G	ENSP00000385185.2:p.Pro1177=
ENST00000445658.6:c.2793C>G	ENSP00000404047.2:p.Pro931=
ENST00000541774.5:c.3576C>G	ENSP00000446466.1:p.Pro1192=
ENST00000578373.5:c.*3411C>G	ENSP00000463427.1:n.*3411C>G
ENST00000584450.5:c.*200C>G	ENSP00000463714.1:n.*200C>G
ENST00000584601.5:c.3531C>G	ENSP00000462438.1:p.Pro1177=
NM_001005862.2:c.3531C>G , LRG_724t1:c.3531C>G	NP_001005862.1:p.Pro1177=
NM_001289936.1:c.3576C>G , LRG_724t4:c.3576C>G	NP_001276865.1:p.Pro1192=
NM_001289937.1:c.*200C>G	NP_001276866.1:n.*200C>G
NM_004448.3:c.3621C>G , LRG_724t2:c.3621C>G	NP_004439.2:p.Pro1207=
NR_110535.1:n.3945C>G
XM_024450641.1:c.3759C>G	XP_024306409.1:p.Pro1253=
XM_024450642.1:c.3714C>G	XP_024306410.1:p.Pro1238=
XM_024450643.1:c.3669C>G	XP_024306411.1:p.Pro1223=
NM_001005862.3:c.3531C>G	NP_001005862.1:p.Pro1177=
NM_001289936.2:c.3576C>G	NP_001276865.1:p.Pro1192=
NM_001289937.2:c.*200C>G	NP_001276866.1:n.*200C>G
NM_001382782.1:c.3531C>G	NP_001369711.1:p.Pro1177=
NM_001382783.1:c.3531C>G	NP_001369712.1:p.Pro1177=
NM_001382784.1:c.3738C>G	NP_001369713.1:p.Pro1246=
NM_001382785.1:c.3723C>G	NP_001369714.1:p.Pro1241=
NM_001382786.1:c.3702C>G	NP_001369715.1:p.Pro1234=
NM_001382787.1:c.3696C>G	NP_001369716.1:p.Pro1232=
NM_001382788.1:c.3651C>G	NP_001369717.1:p.Pro1217=
NM_001382789.1:c.3642C>G	NP_001369718.1:p.Pro1214=
NM_001382790.1:c.3618C>G	NP_001369719.1:p.Pro1206=
NM_001382791.1:c.3612C>G	NP_001369720.1:p.Pro1204=
NM_001382792.1:c.3585C>G	NP_001369721.1:p.Pro1195=
NM_001382793.1:c.3579C>G	NP_001369722.1:p.Pro1193=
NM_001382794.1:c.3579C>G	NP_001369723.1:p.Pro1193=
NM_001382795.1:c.3573C>G	NP_001369724.1:p.Pro1191=
NM_001382796.1:c.3534C>G	NP_001369725.1:p.Pro1178=
NM_001382797.1:c.3522C>G	NP_001369726.1:p.Pro1174=
NM_001382798.1:c.3465C>G	NP_001369727.1:p.Pro1155=
NM_001382799.1:c.3441C>G	NP_001369728.1:p.Pro1147=
NM_001382800.1:c.3435C>G	NP_001369729.1:p.Pro1145=
NM_001382801.1:c.3417C>G	NP_001369730.1:p.Pro1139=
NM_001382802.1:c.3363C>G	NP_001369731.1:p.Pro1121=
NM_001382803.1:c.*200C>G	NP_001369732.1:n.*200C>G
NM_001382804.1:c.2793C>G	NP_001369733.1:p.Pro931=
NM_001382805.1:c.2670C>G	NP_001369734.1:p.Pro890=
NM_001382806.1:c.2583C>G	NP_001369735.1:p.Pro861=
NM_004448.4:c.3621C>G MANE Select	NP_004439.2:p.Pro1207=
NR_110535.2:n.3859C>G