Canonical Allele Identifier: CA499671652

Gene: ERBB2

Linked Data

• gnomAD v4: 17-39727408-A-C
• MyVariant Identifiers: chr17:g.37883661A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727408A>C , CM000679.2:g.39727408A>C	GRCh38
NC_000017.10:g.37883661A>C , CM000679.1:g.37883661A>C	GRCh37
NC_000017.9:g.35137187A>C	NCBI36
NG_007503.1:g.44269A>C , LRG_724:g.44269A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3273A>C MANE Select	ENSP00000269571.4:p.Gly1091=
ENST00000269571.9:c.3273A>C	ENSP00000269571.4:p.Gly1091=
ENST00000406381.6:c.3183A>C	ENSP00000385185.2:p.Gly1061=
ENST00000445658.6:c.2445A>C	ENSP00000404047.2:p.Gly815=
ENST00000541774.5:c.3228A>C	ENSP00000446466.1:p.Gly1076=
ENST00000578373.5:c.*3063A>C	ENSP00000463427.1:n.*3063A>C
ENST00000584450.5:c.3160-281A>C	ENSP00000463714.1:n.3160-281A>C
ENST00000584601.5:c.3183A>C	ENSP00000462438.1:p.Gly1061=
NM_001005862.2:c.3183A>C , LRG_724t1:c.3183A>C	NP_001005862.1:p.Gly1061=
NM_001289936.1:c.3228A>C , LRG_724t4:c.3228A>C	NP_001276865.1:p.Gly1076=
NM_001289937.1:c.3160-281A>C	NP_001276866.1:n.3160-281A>C
NM_004448.3:c.3273A>C , LRG_724t2:c.3273A>C	NP_004439.2:p.Gly1091=
NR_110535.1:n.3597A>C
XM_024450641.1:c.3411A>C	XP_024306409.1:p.Gly1137=
XM_024450642.1:c.3366A>C	XP_024306410.1:p.Gly1122=
XM_024450643.1:c.3321A>C	XP_024306411.1:p.Gly1107=
NM_001005862.3:c.3183A>C	NP_001005862.1:p.Gly1061=
NM_001289936.2:c.3228A>C	NP_001276865.1:p.Gly1076=
NM_001289937.2:c.3160-281A>C	NP_001276866.1:n.3160-281A>C
NM_001382782.1:c.3183A>C	NP_001369711.1:p.Gly1061=
NM_001382783.1:c.3183A>C	NP_001369712.1:p.Gly1061=
NM_001382784.1:c.3390A>C	NP_001369713.1:p.Gly1130=
NM_001382785.1:c.3375A>C	NP_001369714.1:p.Gly1125=
NM_001382786.1:c.3354A>C	NP_001369715.1:p.Gly1118=
NM_001382787.1:c.3348A>C	NP_001369716.1:p.Gly1116=
NM_001382788.1:c.3303A>C	NP_001369717.1:p.Gly1101=
NM_001382789.1:c.3294A>C	NP_001369718.1:p.Gly1098=
NM_001382790.1:c.3270A>C	NP_001369719.1:p.Gly1090=
NM_001382791.1:c.3264A>C	NP_001369720.1:p.Gly1088=
NM_001382792.1:c.3237A>C	NP_001369721.1:p.Gly1079=
NM_001382793.1:c.3231A>C	NP_001369722.1:p.Gly1077=
NM_001382794.1:c.3231A>C	NP_001369723.1:p.Gly1077=
NM_001382795.1:c.3225A>C	NP_001369724.1:p.Gly1075=
NM_001382796.1:c.3186A>C	NP_001369725.1:p.Gly1062=
NM_001382797.1:c.3174A>C	NP_001369726.1:p.Gly1058=
NM_001382798.1:c.3117A>C	NP_001369727.1:p.Gly1039=
NM_001382799.1:c.3093A>C	NP_001369728.1:p.Gly1031=
NM_001382800.1:c.3087A>C	NP_001369729.1:p.Gly1029=
NM_001382801.1:c.3069A>C	NP_001369730.1:p.Gly1023=
NM_001382802.1:c.3015A>C	NP_001369731.1:p.Gly1005=
NM_001382803.1:c.3118-281A>C	NP_001369732.1:n.3118-281A>C
NM_001382804.1:c.2445A>C	NP_001369733.1:p.Gly815=
NM_001382805.1:c.2322A>C	NP_001369734.1:p.Gly774=
NM_001382806.1:c.2235A>C	NP_001369735.1:p.Gly745=
NM_004448.4:c.3273A>C MANE Select	NP_004439.2:p.Gly1091=
NR_110535.2:n.3511A>C