Canonical Allele Identifier: CA399314003

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37884147G>C (hg19) ; chr17:g.39727894G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727894G>C , CM000679.2:g.39727894G>C	GRCh38
NC_000017.10:g.37884147G>C , CM000679.1:g.37884147G>C	GRCh37
NC_000017.9:g.35137673G>C	NCBI36
NG_007503.1:g.44755G>C , LRG_724:g.44755G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3618G>C MANE Select	ENSP00000269571.4:p.Gln1206His
ENST00000269571.9:c.3618G>C	ENSP00000269571.4:p.Gln1206His
ENST00000406381.6:c.3528G>C	ENSP00000385185.2:p.Gln1176His
ENST00000445658.6:c.2790G>C	ENSP00000404047.2:p.Gln930His
ENST00000541774.5:c.3573G>C	ENSP00000446466.1:p.Gln1191His
ENST00000578373.5:c.*3408G>C	ENSP00000463427.1:n.*3408G>C
ENST00000584450.5:c.*197G>C	ENSP00000463714.1:n.*197G>C
ENST00000584601.5:c.3528G>C	ENSP00000462438.1:p.Gln1176His
NM_001005862.2:c.3528G>C , LRG_724t1:c.3528G>C	NP_001005862.1:p.Gln1176His
NM_001289936.1:c.3573G>C , LRG_724t4:c.3573G>C	NP_001276865.1:p.Gln1191His
NM_001289937.1:c.*197G>C	NP_001276866.1:n.*197G>C
NM_004448.3:c.3618G>C , LRG_724t2:c.3618G>C	NP_004439.2:p.Gln1206His
NR_110535.1:n.3942G>C
XM_024450641.1:c.3756G>C	XP_024306409.1:p.Gln1252His
XM_024450642.1:c.3711G>C	XP_024306410.1:p.Gln1237His
XM_024450643.1:c.3666G>C	XP_024306411.1:p.Gln1222His
NM_001005862.3:c.3528G>C	NP_001005862.1:p.Gln1176His
NM_001289936.2:c.3573G>C	NP_001276865.1:p.Gln1191His
NM_001289937.2:c.*197G>C	NP_001276866.1:n.*197G>C
NM_001382782.1:c.3528G>C	NP_001369711.1:p.Gln1176His
NM_001382783.1:c.3528G>C	NP_001369712.1:p.Gln1176His
NM_001382784.1:c.3735G>C	NP_001369713.1:p.Gln1245His
NM_001382785.1:c.3720G>C	NP_001369714.1:p.Gln1240His
NM_001382786.1:c.3699G>C	NP_001369715.1:p.Gln1233His
NM_001382787.1:c.3693G>C	NP_001369716.1:p.Gln1231His
NM_001382788.1:c.3648G>C	NP_001369717.1:p.Gln1216His
NM_001382789.1:c.3639G>C	NP_001369718.1:p.Gln1213His
NM_001382790.1:c.3615G>C	NP_001369719.1:p.Gln1205His
NM_001382791.1:c.3609G>C	NP_001369720.1:p.Gln1203His
NM_001382792.1:c.3582G>C	NP_001369721.1:p.Gln1194His
NM_001382793.1:c.3576G>C	NP_001369722.1:p.Gln1192His
NM_001382794.1:c.3576G>C	NP_001369723.1:p.Gln1192His
NM_001382795.1:c.3570G>C	NP_001369724.1:p.Gln1190His
NM_001382796.1:c.3531G>C	NP_001369725.1:p.Gln1177His
NM_001382797.1:c.3519G>C	NP_001369726.1:p.Gln1173His
NM_001382798.1:c.3462G>C	NP_001369727.1:p.Gln1154His
NM_001382799.1:c.3438G>C	NP_001369728.1:p.Gln1146His
NM_001382800.1:c.3432G>C	NP_001369729.1:p.Gln1144His
NM_001382801.1:c.3414G>C	NP_001369730.1:p.Gln1138His
NM_001382802.1:c.3360G>C	NP_001369731.1:p.Gln1120His
NM_001382803.1:c.*197G>C	NP_001369732.1:n.*197G>C
NM_001382804.1:c.2790G>C	NP_001369733.1:p.Gln930His
NM_001382805.1:c.2667G>C	NP_001369734.1:p.Gln889His
NM_001382806.1:c.2580G>C	NP_001369735.1:p.Gln860His
NM_004448.4:c.3618G>C MANE Select	NP_004439.2:p.Gln1206His
NR_110535.2:n.3856G>C