Canonical Allele Identifier: CA499671614

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143238610
• MyVariant Identifiers: chr17:g.37883610A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727357A>T , CM000679.2:g.39727357A>T	GRCh38
NC_000017.10:g.37883610A>T , CM000679.1:g.37883610A>T	GRCh37
NC_000017.9:g.35137136A>T	NCBI36
NG_007503.1:g.44218A>T , LRG_724:g.44218A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3222A>T MANE Select	ENSP00000269571.4:p.Pro1074=
ENST00000269571.9:c.3222A>T	ENSP00000269571.4:p.Pro1074=
ENST00000406381.6:c.3132A>T	ENSP00000385185.2:p.Pro1044=
ENST00000445658.6:c.2394A>T	ENSP00000404047.2:p.Pro798=
ENST00000541774.5:c.3177A>T	ENSP00000446466.1:p.Pro1059=
ENST00000578373.5:c.*3012A>T	ENSP00000463427.1:n.*3012A>T
ENST00000584450.5:c.3160-332A>T	ENSP00000463714.1:n.3160-332A>T
ENST00000584601.5:c.3132A>T	ENSP00000462438.1:p.Pro1044=
NM_001005862.2:c.3132A>T , LRG_724t1:c.3132A>T	NP_001005862.1:p.Pro1044=
NM_001289936.1:c.3177A>T , LRG_724t4:c.3177A>T	NP_001276865.1:p.Pro1059=
NM_001289937.1:c.3160-332A>T	NP_001276866.1:n.3160-332A>T
NM_004448.3:c.3222A>T , LRG_724t2:c.3222A>T	NP_004439.2:p.Pro1074=
NR_110535.1:n.3546A>T
XM_024450641.1:c.3360A>T	XP_024306409.1:p.Pro1120=
XM_024450642.1:c.3315A>T	XP_024306410.1:p.Pro1105=
XM_024450643.1:c.3270A>T	XP_024306411.1:p.Pro1090=
NM_001005862.3:c.3132A>T	NP_001005862.1:p.Pro1044=
NM_001289936.2:c.3177A>T	NP_001276865.1:p.Pro1059=
NM_001289937.2:c.3160-332A>T	NP_001276866.1:n.3160-332A>T
NM_001382782.1:c.3132A>T	NP_001369711.1:p.Pro1044=
NM_001382783.1:c.3132A>T	NP_001369712.1:p.Pro1044=
NM_001382784.1:c.3339A>T	NP_001369713.1:p.Pro1113=
NM_001382785.1:c.3324A>T	NP_001369714.1:p.Pro1108=
NM_001382786.1:c.3303A>T	NP_001369715.1:p.Pro1101=
NM_001382787.1:c.3297A>T	NP_001369716.1:p.Pro1099=
NM_001382788.1:c.3252A>T	NP_001369717.1:p.Pro1084=
NM_001382789.1:c.3243A>T	NP_001369718.1:p.Pro1081=
NM_001382790.1:c.3219A>T	NP_001369719.1:p.Pro1073=
NM_001382791.1:c.3213A>T	NP_001369720.1:p.Pro1071=
NM_001382792.1:c.3186A>T	NP_001369721.1:p.Pro1062=
NM_001382793.1:c.3180A>T	NP_001369722.1:p.Pro1060=
NM_001382794.1:c.3180A>T	NP_001369723.1:p.Pro1060=
NM_001382795.1:c.3174A>T	NP_001369724.1:p.Pro1058=
NM_001382796.1:c.3135A>T	NP_001369725.1:p.Pro1045=
NM_001382797.1:c.3123A>T	NP_001369726.1:p.Pro1041=
NM_001382798.1:c.3066A>T	NP_001369727.1:p.Pro1022=
NM_001382799.1:c.3042A>T	NP_001369728.1:p.Pro1014=
NM_001382800.1:c.3036A>T	NP_001369729.1:p.Pro1012=
NM_001382801.1:c.3018A>T	NP_001369730.1:p.Pro1006=
NM_001382802.1:c.2964A>T	NP_001369731.1:p.Pro988=
NM_001382803.1:c.3118-332A>T	NP_001369732.1:n.3118-332A>T
NM_001382804.1:c.2394A>T	NP_001369733.1:p.Pro798=
NM_001382805.1:c.2271A>T	NP_001369734.1:p.Pro757=
NM_001382806.1:c.2184A>T	NP_001369735.1:p.Pro728=
NM_004448.4:c.3222A>T MANE Select	NP_004439.2:p.Pro1074=
NR_110535.2:n.3460A>T