Canonical Allele Identifier: CA499890274

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37883754T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727501T>G , CM000679.2:g.39727501T>G	GRCh38
NC_000017.10:g.37883754T>G , CM000679.1:g.37883754T>G	GRCh37
NC_000017.9:g.35137280T>G	NCBI36
NG_007503.1:g.44362T>G , LRG_724:g.44362T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3366T>G MANE Select	ENSP00000269571.4:p.Ser1122=
ENST00000269571.9:c.3366T>G	ENSP00000269571.4:p.Ser1122=
ENST00000406381.6:c.3276T>G	ENSP00000385185.2:p.Ser1092=
ENST00000445658.6:c.2538T>G	ENSP00000404047.2:p.Ser846=
ENST00000541774.5:c.3321T>G	ENSP00000446466.1:p.Ser1107=
ENST00000578373.5:c.*3156T>G	ENSP00000463427.1:n.*3156T>G
ENST00000584450.5:c.3160-188T>G	ENSP00000463714.1:n.3160-188T>G
ENST00000584601.5:c.3276T>G	ENSP00000462438.1:p.Ser1092=
NM_001005862.2:c.3276T>G , LRG_724t1:c.3276T>G	NP_001005862.1:p.Ser1092=
NM_001289936.1:c.3321T>G , LRG_724t4:c.3321T>G	NP_001276865.1:p.Ser1107=
NM_001289937.1:c.3160-188T>G	NP_001276866.1:n.3160-188T>G
NM_004448.3:c.3366T>G , LRG_724t2:c.3366T>G	NP_004439.2:p.Ser1122=
NR_110535.1:n.3690T>G
XM_024450641.1:c.3504T>G	XP_024306409.1:p.Ser1168=
XM_024450642.1:c.3459T>G	XP_024306410.1:p.Ser1153=
XM_024450643.1:c.3414T>G	XP_024306411.1:p.Ser1138=
NM_001005862.3:c.3276T>G	NP_001005862.1:p.Ser1092=
NM_001289936.2:c.3321T>G	NP_001276865.1:p.Ser1107=
NM_001289937.2:c.3160-188T>G	NP_001276866.1:n.3160-188T>G
NM_001382782.1:c.3276T>G	NP_001369711.1:p.Ser1092=
NM_001382783.1:c.3276T>G	NP_001369712.1:p.Ser1092=
NM_001382784.1:c.3483T>G	NP_001369713.1:p.Ser1161=
NM_001382785.1:c.3468T>G	NP_001369714.1:p.Ser1156=
NM_001382786.1:c.3447T>G	NP_001369715.1:p.Ser1149=
NM_001382787.1:c.3441T>G	NP_001369716.1:p.Ser1147=
NM_001382788.1:c.3396T>G	NP_001369717.1:p.Ser1132=
NM_001382789.1:c.3387T>G	NP_001369718.1:p.Ser1129=
NM_001382790.1:c.3363T>G	NP_001369719.1:p.Ser1121=
NM_001382791.1:c.3357T>G	NP_001369720.1:p.Ser1119=
NM_001382792.1:c.3330T>G	NP_001369721.1:p.Ser1110=
NM_001382793.1:c.3324T>G	NP_001369722.1:p.Ser1108=
NM_001382794.1:c.3324T>G	NP_001369723.1:p.Ser1108=
NM_001382795.1:c.3318T>G	NP_001369724.1:p.Ser1106=
NM_001382796.1:c.3279T>G	NP_001369725.1:p.Ser1093=
NM_001382797.1:c.3267T>G	NP_001369726.1:p.Ser1089=
NM_001382798.1:c.3210T>G	NP_001369727.1:p.Ser1070=
NM_001382799.1:c.3186T>G	NP_001369728.1:p.Ser1062=
NM_001382800.1:c.3180T>G	NP_001369729.1:p.Ser1060=
NM_001382801.1:c.3162T>G	NP_001369730.1:p.Ser1054=
NM_001382802.1:c.3108T>G	NP_001369731.1:p.Ser1036=
NM_001382803.1:c.3118-188T>G	NP_001369732.1:n.3118-188T>G
NM_001382804.1:c.2538T>G	NP_001369733.1:p.Ser846=
NM_001382805.1:c.2415T>G	NP_001369734.1:p.Ser805=
NM_001382806.1:c.2328T>G	NP_001369735.1:p.Ser776=
NM_004448.4:c.3366T>G MANE Select	NP_004439.2:p.Ser1122=
NR_110535.2:n.3604T>G