Canonical Allele Identifier: CA499890572

Gene: ERBB2

Linked Data

• gnomAD v4: 17-39727744-T-C
• MyVariant Identifiers: chr17:g.37883997T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727744T>C , CM000679.2:g.39727744T>C	GRCh38
NC_000017.10:g.37883997T>C , CM000679.1:g.37883997T>C	GRCh37
NC_000017.9:g.35137523T>C	NCBI36
NG_007503.1:g.44605T>C , LRG_724:g.44605T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3468T>C MANE Select	ENSP00000269571.4:p.Pro1156=
ENST00000269571.9:c.3468T>C	ENSP00000269571.4:p.Pro1156=
ENST00000406381.6:c.3378T>C	ENSP00000385185.2:p.Pro1126=
ENST00000445658.6:c.2640T>C	ENSP00000404047.2:p.Pro880=
ENST00000541774.5:c.3423T>C	ENSP00000446466.1:p.Pro1141=
ENST00000578373.5:c.*3258T>C	ENSP00000463427.1:n.*3258T>C
ENST00000584450.5:c.*47T>C	ENSP00000463714.1:n.*47T>C
ENST00000584601.5:c.3378T>C	ENSP00000462438.1:p.Pro1126=
NM_001005862.2:c.3378T>C , LRG_724t1:c.3378T>C	NP_001005862.1:p.Pro1126=
NM_001289936.1:c.3423T>C , LRG_724t4:c.3423T>C	NP_001276865.1:p.Pro1141=
NM_001289937.1:c.*47T>C	NP_001276866.1:n.*47T>C
NM_004448.3:c.3468T>C , LRG_724t2:c.3468T>C	NP_004439.2:p.Pro1156=
NR_110535.1:n.3792T>C
XM_024450641.1:c.3606T>C	XP_024306409.1:p.Pro1202=
XM_024450642.1:c.3561T>C	XP_024306410.1:p.Pro1187=
XM_024450643.1:c.3516T>C	XP_024306411.1:p.Pro1172=
NM_001005862.3:c.3378T>C	NP_001005862.1:p.Pro1126=
NM_001289936.2:c.3423T>C	NP_001276865.1:p.Pro1141=
NM_001289937.2:c.*47T>C	NP_001276866.1:n.*47T>C
NM_001382782.1:c.3378T>C	NP_001369711.1:p.Pro1126=
NM_001382783.1:c.3378T>C	NP_001369712.1:p.Pro1126=
NM_001382784.1:c.3585T>C	NP_001369713.1:p.Pro1195=
NM_001382785.1:c.3570T>C	NP_001369714.1:p.Pro1190=
NM_001382786.1:c.3549T>C	NP_001369715.1:p.Pro1183=
NM_001382787.1:c.3543T>C	NP_001369716.1:p.Pro1181=
NM_001382788.1:c.3498T>C	NP_001369717.1:p.Pro1166=
NM_001382789.1:c.3489T>C	NP_001369718.1:p.Pro1163=
NM_001382790.1:c.3465T>C	NP_001369719.1:p.Pro1155=
NM_001382791.1:c.3459T>C	NP_001369720.1:p.Pro1153=
NM_001382792.1:c.3432T>C	NP_001369721.1:p.Pro1144=
NM_001382793.1:c.3426T>C	NP_001369722.1:p.Pro1142=
NM_001382794.1:c.3426T>C	NP_001369723.1:p.Pro1142=
NM_001382795.1:c.3420T>C	NP_001369724.1:p.Pro1140=
NM_001382796.1:c.3381T>C	NP_001369725.1:p.Pro1127=
NM_001382797.1:c.3369T>C	NP_001369726.1:p.Pro1123=
NM_001382798.1:c.3312T>C	NP_001369727.1:p.Pro1104=
NM_001382799.1:c.3288T>C	NP_001369728.1:p.Pro1096=
NM_001382800.1:c.3282T>C	NP_001369729.1:p.Pro1094=
NM_001382801.1:c.3264T>C	NP_001369730.1:p.Pro1088=
NM_001382802.1:c.3210T>C	NP_001369731.1:p.Pro1070=
NM_001382803.1:c.*47T>C	NP_001369732.1:n.*47T>C
NM_001382804.1:c.2640T>C	NP_001369733.1:p.Pro880=
NM_001382805.1:c.2517T>C	NP_001369734.1:p.Pro839=
NM_001382806.1:c.2430T>C	NP_001369735.1:p.Pro810=
NM_004448.4:c.3468T>C MANE Select	NP_004439.2:p.Pro1156=
NR_110535.2:n.3706T>C