Canonical Allele Identifier: CA499671625

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37883619C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727366C>T , CM000679.2:g.39727366C>T	GRCh38
NC_000017.10:g.37883619C>T , CM000679.1:g.37883619C>T	GRCh37
NC_000017.9:g.35137145C>T	NCBI36
NG_007503.1:g.44227C>T , LRG_724:g.44227C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3231C>T MANE Select	ENSP00000269571.4:p.Pro1077=
ENST00000269571.9:c.3231C>T	ENSP00000269571.4:p.Pro1077=
ENST00000406381.6:c.3141C>T	ENSP00000385185.2:p.Pro1047=
ENST00000445658.6:c.2403C>T	ENSP00000404047.2:p.Pro801=
ENST00000541774.5:c.3186C>T	ENSP00000446466.1:p.Pro1062=
ENST00000578373.5:c.*3021C>T	ENSP00000463427.1:n.*3021C>T
ENST00000584450.5:c.3160-323C>T	ENSP00000463714.1:n.3160-323C>T
ENST00000584601.5:c.3141C>T	ENSP00000462438.1:p.Pro1047=
NM_001005862.2:c.3141C>T , LRG_724t1:c.3141C>T	NP_001005862.1:p.Pro1047=
NM_001289936.1:c.3186C>T , LRG_724t4:c.3186C>T	NP_001276865.1:p.Pro1062=
NM_001289937.1:c.3160-323C>T	NP_001276866.1:n.3160-323C>T
NM_004448.3:c.3231C>T , LRG_724t2:c.3231C>T	NP_004439.2:p.Pro1077=
NR_110535.1:n.3555C>T
XM_024450641.1:c.3369C>T	XP_024306409.1:p.Pro1123=
XM_024450642.1:c.3324C>T	XP_024306410.1:p.Pro1108=
XM_024450643.1:c.3279C>T	XP_024306411.1:p.Pro1093=
NM_001005862.3:c.3141C>T	NP_001005862.1:p.Pro1047=
NM_001289936.2:c.3186C>T	NP_001276865.1:p.Pro1062=
NM_001289937.2:c.3160-323C>T	NP_001276866.1:n.3160-323C>T
NM_001382782.1:c.3141C>T	NP_001369711.1:p.Pro1047=
NM_001382783.1:c.3141C>T	NP_001369712.1:p.Pro1047=
NM_001382784.1:c.3348C>T	NP_001369713.1:p.Pro1116=
NM_001382785.1:c.3333C>T	NP_001369714.1:p.Pro1111=
NM_001382786.1:c.3312C>T	NP_001369715.1:p.Pro1104=
NM_001382787.1:c.3306C>T	NP_001369716.1:p.Pro1102=
NM_001382788.1:c.3261C>T	NP_001369717.1:p.Pro1087=
NM_001382789.1:c.3252C>T	NP_001369718.1:p.Pro1084=
NM_001382790.1:c.3228C>T	NP_001369719.1:p.Pro1076=
NM_001382791.1:c.3222C>T	NP_001369720.1:p.Pro1074=
NM_001382792.1:c.3195C>T	NP_001369721.1:p.Pro1065=
NM_001382793.1:c.3189C>T	NP_001369722.1:p.Pro1063=
NM_001382794.1:c.3189C>T	NP_001369723.1:p.Pro1063=
NM_001382795.1:c.3183C>T	NP_001369724.1:p.Pro1061=
NM_001382796.1:c.3144C>T	NP_001369725.1:p.Pro1048=
NM_001382797.1:c.3132C>T	NP_001369726.1:p.Pro1044=
NM_001382798.1:c.3075C>T	NP_001369727.1:p.Pro1025=
NM_001382799.1:c.3051C>T	NP_001369728.1:p.Pro1017=
NM_001382800.1:c.3045C>T	NP_001369729.1:p.Pro1015=
NM_001382801.1:c.3027C>T	NP_001369730.1:p.Pro1009=
NM_001382802.1:c.2973C>T	NP_001369731.1:p.Pro991=
NM_001382803.1:c.3118-323C>T	NP_001369732.1:n.3118-323C>T
NM_001382804.1:c.2403C>T	NP_001369733.1:p.Pro801=
NM_001382805.1:c.2280C>T	NP_001369734.1:p.Pro760=
NM_001382806.1:c.2193C>T	NP_001369735.1:p.Pro731=
NM_004448.4:c.3231C>T MANE Select	NP_004439.2:p.Pro1077=
NR_110535.2:n.3469C>T