Canonical Allele Identifier: CA499670907

Gene: ERBB2

Linked Data

• gnomAD v4: 17-39724833-C-T
• MyVariant Identifiers: chr17:g.37881086C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39724833C>T , CM000679.2:g.39724833C>T	GRCh38
NC_000017.10:g.37881086C>T , CM000679.1:g.37881086C>T	GRCh37
NC_000017.9:g.35134612C>T	NCBI36
NG_007503.1:g.41694C>T , LRG_724:g.41694C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2415C>T MANE Select	ENSP00000269571.4:p.Cys805=
ENST00000269571.9:c.2415C>T	ENSP00000269571.4:p.Cys805=
ENST00000406381.6:c.2325C>T	ENSP00000385185.2:p.Cys775=
ENST00000445658.6:c.1587C>T	ENSP00000404047.2:p.Cys529=
ENST00000541774.5:c.2370C>T	ENSP00000446466.1:p.Cys790=
ENST00000578373.5:c.*2205C>T	ENSP00000463427.1:n.*2205C>T
ENST00000580074.1:c.521C>T
ENST00000583038.5:n.3549C>T
ENST00000584450.5:c.2415C>T	ENSP00000463714.1:p.Cys805=
ENST00000584601.5:c.2325C>T	ENSP00000462438.1:p.Cys775=
NM_001005862.2:c.2325C>T , LRG_724t1:c.2325C>T	NP_001005862.1:p.Cys775=
NM_001289936.1:c.2370C>T , LRG_724t4:c.2370C>T	NP_001276865.1:p.Cys790=
NM_001289937.1:c.2415C>T	NP_001276866.1:p.Cys805=
NM_004448.3:c.2415C>T , LRG_724t2:c.2415C>T	NP_004439.2:p.Cys805=
NR_110535.1:n.2739C>T
XM_024450641.1:c.2553C>T	XP_024306409.1:p.Cys851=
XM_024450642.1:c.2508C>T	XP_024306410.1:p.Cys836=
XM_024450643.1:c.2463C>T	XP_024306411.1:p.Cys821=
NM_001005862.3:c.2325C>T	NP_001005862.1:p.Cys775=
NM_001289936.2:c.2370C>T	NP_001276865.1:p.Cys790=
NM_001289937.2:c.2415C>T	NP_001276866.1:p.Cys805=
NM_001382782.1:c.2325C>T	NP_001369711.1:p.Cys775=
NM_001382783.1:c.2325C>T	NP_001369712.1:p.Cys775=
NM_001382784.1:c.2532C>T	NP_001369713.1:p.Cys844=
NM_001382785.1:c.2517C>T	NP_001369714.1:p.Cys839=
NM_001382786.1:c.2496C>T	NP_001369715.1:p.Cys832=
NM_001382787.1:c.2490C>T	NP_001369716.1:p.Cys830=
NM_001382788.1:c.2445C>T	NP_001369717.1:p.Cys815=
NM_001382789.1:c.2436C>T	NP_001369718.1:p.Cys812=
NM_001382790.1:c.2412C>T	NP_001369719.1:p.Cys804=
NM_001382791.1:c.2406C>T	NP_001369720.1:p.Cys802=
NM_001382792.1:c.2379C>T	NP_001369721.1:p.Cys793=
NM_001382793.1:c.2373C>T	NP_001369722.1:p.Cys791=
NM_001382794.1:c.2373C>T	NP_001369723.1:p.Cys791=
NM_001382795.1:c.2367C>T	NP_001369724.1:p.Cys789=
NM_001382796.1:c.2415C>T	NP_001369725.1:p.Cys805=
NM_001382797.1:c.2316C>T	NP_001369726.1:p.Cys772=
NM_001382798.1:c.2415C>T	NP_001369727.1:p.Cys805=
NM_001382799.1:c.2235C>T	NP_001369728.1:p.Cys745=
NM_001382800.1:c.2308-216C>T	NP_001369729.1:n.2308-216C>T
NM_001382801.1:c.2367C>T	NP_001369730.1:p.Cys789=
NM_001382802.1:c.2157C>T	NP_001369731.1:p.Cys719=
NM_001382803.1:c.2373C>T	NP_001369732.1:p.Cys791=
NM_001382804.1:c.1587C>T	NP_001369733.1:p.Cys529=
NM_001382805.1:c.2208+1173C>T	NP_001369734.1:n.2208+1173C>T
NM_001382806.1:c.1377C>T	NP_001369735.1:p.Cys459=
NM_004448.4:c.2415C>T MANE Select	NP_004439.2:p.Cys805=
NR_110535.2:n.2653C>T