Canonical Allele Identifier: CA399312841

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143287482
• MyVariant Identifiers: chr17:g.37883951A>T (hg19) ; chr17:g.39727698A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727698A>T , CM000679.2:g.39727698A>T	GRCh38
NC_000017.10:g.37883951A>T , CM000679.1:g.37883951A>T	GRCh37
NC_000017.9:g.35137477A>T	NCBI36
NG_007503.1:g.44559A>T , LRG_724:g.44559A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000269571.10:c.3422A>T MANE Select	ENSP00000269571.4:p.Asn1141Ile
ENST00000269571.9:c.3422A>T	ENSP00000269571.4:p.Asn1141Ile
ENST00000406381.6:c.3332A>T	ENSP00000385185.2:p.Asn1111Ile
ENST00000445658.6:c.2594A>T	ENSP00000404047.2:p.Asn865Ile
ENST00000541774.5:c.3377A>T	ENSP00000446466.1:p.Asn1126Ile
ENST00000578373.5:c.*3212A>T	ENSP00000463427.1:n.*3212A>T
ENST00000584450.5:c.*1A>T	ENSP00000463714.1:n.*1A>T
ENST00000584601.5:c.3332A>T	ENSP00000462438.1:p.Asn1111Ile
NM_001005862.2:c.3332A>T , LRG_724t1:c.3332A>T	NP_001005862.1:p.Asn1111Ile
NM_001289936.1:c.3377A>T , LRG_724t4:c.3377A>T	NP_001276865.1:p.Asn1126Ile
NM_001289937.1:c.*1A>T	NP_001276866.1:n.*1A>T
NM_004448.3:c.3422A>T , LRG_724t2:c.3422A>T	NP_004439.2:p.Asn1141Ile
NR_110535.1:n.3746A>T
XM_024450641.1:c.3560A>T	XP_024306409.1:p.Asn1187Ile
XM_024450642.1:c.3515A>T	XP_024306410.1:p.Asn1172Ile
XM_024450643.1:c.3470A>T	XP_024306411.1:p.Asn1157Ile
NM_001005862.3:c.3332A>T	NP_001005862.1:p.Asn1111Ile
NM_001289936.2:c.3377A>T	NP_001276865.1:p.Asn1126Ile
NM_001289937.2:c.*1A>T	NP_001276866.1:n.*1A>T
NM_001382782.1:c.3332A>T	NP_001369711.1:p.Asn1111Ile
NM_001382783.1:c.3332A>T	NP_001369712.1:p.Asn1111Ile
NM_001382784.1:c.3539A>T	NP_001369713.1:p.Asn1180Ile
NM_001382785.1:c.3524A>T	NP_001369714.1:p.Asn1175Ile
NM_001382786.1:c.3503A>T	NP_001369715.1:p.Asn1168Ile
NM_001382787.1:c.3497A>T	NP_001369716.1:p.Asn1166Ile
NM_001382788.1:c.3452A>T	NP_001369717.1:p.Asn1151Ile
NM_001382789.1:c.3443A>T	NP_001369718.1:p.Asn1148Ile
NM_001382790.1:c.3419A>T	NP_001369719.1:p.Asn1140Ile
NM_001382791.1:c.3413A>T	NP_001369720.1:p.Asn1138Ile
NM_001382792.1:c.3386A>T	NP_001369721.1:p.Asn1129Ile
NM_001382793.1:c.3380A>T	NP_001369722.1:p.Asn1127Ile
NM_001382794.1:c.3380A>T	NP_001369723.1:p.Asn1127Ile
NM_001382795.1:c.3374A>T	NP_001369724.1:p.Asn1125Ile
NM_001382796.1:c.3335A>T	NP_001369725.1:p.Asn1112Ile
NM_001382797.1:c.3323A>T	NP_001369726.1:p.Asn1108Ile
NM_001382798.1:c.3266A>T	NP_001369727.1:p.Asn1089Ile
NM_001382799.1:c.3242A>T	NP_001369728.1:p.Asn1081Ile
NM_001382800.1:c.3236A>T	NP_001369729.1:p.Asn1079Ile
NM_001382801.1:c.3218A>T	NP_001369730.1:p.Asn1073Ile
NM_001382802.1:c.3164A>T	NP_001369731.1:p.Asn1055Ile
NM_001382803.1:c.*1A>T	NP_001369732.1:n.*1A>T
NM_001382804.1:c.2594A>T	NP_001369733.1:p.Asn865Ile
NM_001382805.1:c.2471A>T	NP_001369734.1:p.Asn824Ile
NM_001382806.1:c.2384A>T	NP_001369735.1:p.Asn795Ile
NM_004448.4:c.3422A>T MANE Select	NP_004439.2:p.Asn1141Ile
NR_110535.2:n.3660A>T