Canonical Allele Identifier: CA499890082

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37881316G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39725063G>T , CM000679.2:g.39725063G>T	GRCh38
NC_000017.10:g.37881316G>T , CM000679.1:g.37881316G>T	GRCh37
NC_000017.9:g.35134842G>T	NCBI36
NG_007503.1:g.41924G>T , LRG_724:g.41924G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2508G>T MANE Select	ENSP00000269571.4:p.Leu836=
ENST00000269571.9:c.2508G>T	ENSP00000269571.4:p.Leu836=
ENST00000406381.6:c.2418G>T	ENSP00000385185.2:p.Leu806=
ENST00000445658.6:c.1680G>T	ENSP00000404047.2:p.Leu560=
ENST00000541774.5:c.2463G>T	ENSP00000446466.1:p.Leu821=
ENST00000578373.5:c.*2298G>T	ENSP00000463427.1:n.*2298G>T
ENST00000580074.1:c.614G>T
ENST00000583038.5:n.3642G>T
ENST00000584450.5:c.2508G>T	ENSP00000463714.1:p.Leu836=
ENST00000584601.5:c.2418G>T	ENSP00000462438.1:p.Leu806=
NM_001005862.2:c.2418G>T , LRG_724t1:c.2418G>T	NP_001005862.1:p.Leu806=
NM_001289936.1:c.2463G>T , LRG_724t4:c.2463G>T	NP_001276865.1:p.Leu821=
NM_001289937.1:c.2508G>T	NP_001276866.1:p.Leu836=
NM_004448.3:c.2508G>T , LRG_724t2:c.2508G>T	NP_004439.2:p.Leu836=
NR_110535.1:n.2832G>T
XM_024450641.1:c.2646G>T	XP_024306409.1:p.Leu882=
XM_024450642.1:c.2601G>T	XP_024306410.1:p.Leu867=
XM_024450643.1:c.2556G>T	XP_024306411.1:p.Leu852=
NM_001005862.3:c.2418G>T	NP_001005862.1:p.Leu806=
NM_001289936.2:c.2463G>T	NP_001276865.1:p.Leu821=
NM_001289937.2:c.2508G>T	NP_001276866.1:p.Leu836=
NM_001382782.1:c.2418G>T	NP_001369711.1:p.Leu806=
NM_001382783.1:c.2418G>T	NP_001369712.1:p.Leu806=
NM_001382784.1:c.2625G>T	NP_001369713.1:p.Leu875=
NM_001382785.1:c.2610G>T	NP_001369714.1:p.Leu870=
NM_001382786.1:c.2589G>T	NP_001369715.1:p.Leu863=
NM_001382787.1:c.2583G>T	NP_001369716.1:p.Leu861=
NM_001382788.1:c.2538G>T	NP_001369717.1:p.Leu846=
NM_001382789.1:c.2529G>T	NP_001369718.1:p.Leu843=
NM_001382790.1:c.2505G>T	NP_001369719.1:p.Leu835=
NM_001382791.1:c.2499G>T	NP_001369720.1:p.Leu833=
NM_001382792.1:c.2472G>T	NP_001369721.1:p.Leu824=
NM_001382793.1:c.2466G>T	NP_001369722.1:p.Leu822=
NM_001382794.1:c.2466G>T	NP_001369723.1:p.Leu822=
NM_001382795.1:c.2460G>T	NP_001369724.1:p.Leu820=
NM_001382796.1:c.2508G>T	NP_001369725.1:p.Leu836=
NM_001382797.1:c.2409G>T	NP_001369726.1:p.Leu803=
NM_001382798.1:c.2493+152G>T	NP_001369727.1:n.2493+152G>T
NM_001382799.1:c.2328G>T	NP_001369728.1:p.Leu776=
NM_001382800.1:c.2322G>T	NP_001369729.1:p.Leu774=
NM_001382801.1:c.2445+152G>T	NP_001369730.1:n.2445+152G>T
NM_001382802.1:c.2250G>T	NP_001369731.1:p.Leu750=
NM_001382803.1:c.2466G>T	NP_001369732.1:p.Leu822=
NM_001382804.1:c.1680G>T	NP_001369733.1:p.Leu560=
NM_001382805.1:c.2208+1403G>T	NP_001369734.1:n.2208+1403G>T
NM_001382806.1:c.1470G>T	NP_001369735.1:p.Leu490=
NM_004448.4:c.2508G>T MANE Select	NP_004439.2:p.Leu836=
NR_110535.2:n.2746G>T