Canonical Allele Identifier: CA499890256

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37883736C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727483C>G , CM000679.2:g.39727483C>G	GRCh38
NC_000017.10:g.37883736C>G , CM000679.1:g.37883736C>G	GRCh37
NC_000017.9:g.35137262C>G	NCBI36
NG_007503.1:g.44344C>G , LRG_724:g.44344C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3348C>G MANE Select	ENSP00000269571.4:p.Pro1116=
ENST00000269571.9:c.3348C>G	ENSP00000269571.4:p.Pro1116=
ENST00000406381.6:c.3258C>G	ENSP00000385185.2:p.Pro1086=
ENST00000445658.6:c.2520C>G	ENSP00000404047.2:p.Pro840=
ENST00000541774.5:c.3303C>G	ENSP00000446466.1:p.Pro1101=
ENST00000578373.5:c.*3138C>G	ENSP00000463427.1:n.*3138C>G
ENST00000584450.5:c.3160-206C>G	ENSP00000463714.1:n.3160-206C>G
ENST00000584601.5:c.3258C>G	ENSP00000462438.1:p.Pro1086=
NM_001005862.2:c.3258C>G , LRG_724t1:c.3258C>G	NP_001005862.1:p.Pro1086=
NM_001289936.1:c.3303C>G , LRG_724t4:c.3303C>G	NP_001276865.1:p.Pro1101=
NM_001289937.1:c.3160-206C>G	NP_001276866.1:n.3160-206C>G
NM_004448.3:c.3348C>G , LRG_724t2:c.3348C>G	NP_004439.2:p.Pro1116=
NR_110535.1:n.3672C>G
XM_024450641.1:c.3486C>G	XP_024306409.1:p.Pro1162=
XM_024450642.1:c.3441C>G	XP_024306410.1:p.Pro1147=
XM_024450643.1:c.3396C>G	XP_024306411.1:p.Pro1132=
NM_001005862.3:c.3258C>G	NP_001005862.1:p.Pro1086=
NM_001289936.2:c.3303C>G	NP_001276865.1:p.Pro1101=
NM_001289937.2:c.3160-206C>G	NP_001276866.1:n.3160-206C>G
NM_001382782.1:c.3258C>G	NP_001369711.1:p.Pro1086=
NM_001382783.1:c.3258C>G	NP_001369712.1:p.Pro1086=
NM_001382784.1:c.3465C>G	NP_001369713.1:p.Pro1155=
NM_001382785.1:c.3450C>G	NP_001369714.1:p.Pro1150=
NM_001382786.1:c.3429C>G	NP_001369715.1:p.Pro1143=
NM_001382787.1:c.3423C>G	NP_001369716.1:p.Pro1141=
NM_001382788.1:c.3378C>G	NP_001369717.1:p.Pro1126=
NM_001382789.1:c.3369C>G	NP_001369718.1:p.Pro1123=
NM_001382790.1:c.3345C>G	NP_001369719.1:p.Pro1115=
NM_001382791.1:c.3339C>G	NP_001369720.1:p.Pro1113=
NM_001382792.1:c.3312C>G	NP_001369721.1:p.Pro1104=
NM_001382793.1:c.3306C>G	NP_001369722.1:p.Pro1102=
NM_001382794.1:c.3306C>G	NP_001369723.1:p.Pro1102=
NM_001382795.1:c.3300C>G	NP_001369724.1:p.Pro1100=
NM_001382796.1:c.3261C>G	NP_001369725.1:p.Pro1087=
NM_001382797.1:c.3249C>G	NP_001369726.1:p.Pro1083=
NM_001382798.1:c.3192C>G	NP_001369727.1:p.Pro1064=
NM_001382799.1:c.3168C>G	NP_001369728.1:p.Pro1056=
NM_001382800.1:c.3162C>G	NP_001369729.1:p.Pro1054=
NM_001382801.1:c.3144C>G	NP_001369730.1:p.Pro1048=
NM_001382802.1:c.3090C>G	NP_001369731.1:p.Pro1030=
NM_001382803.1:c.3118-206C>G	NP_001369732.1:n.3118-206C>G
NM_001382804.1:c.2520C>G	NP_001369733.1:p.Pro840=
NM_001382805.1:c.2397C>G	NP_001369734.1:p.Pro799=
NM_001382806.1:c.2310C>G	NP_001369735.1:p.Pro770=
NM_004448.4:c.3348C>G MANE Select	NP_004439.2:p.Pro1116=
NR_110535.2:n.3586C>G