Canonical Allele Identifier: CA499671595

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143235402
• MyVariant Identifiers: chr17:g.37883583C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727330C>A , CM000679.2:g.39727330C>A	GRCh38
NC_000017.10:g.37883583C>A , CM000679.1:g.37883583C>A	GRCh37
NC_000017.9:g.35137109C>A	NCBI36
NG_007503.1:g.44191C>A , LRG_724:g.44191C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3195C>A MANE Select	ENSP00000269571.4:p.Pro1065=
ENST00000269571.9:c.3195C>A	ENSP00000269571.4:p.Pro1065=
ENST00000406381.6:c.3105C>A	ENSP00000385185.2:p.Pro1035=
ENST00000445658.6:c.2367C>A	ENSP00000404047.2:p.Pro789=
ENST00000541774.5:c.3150C>A	ENSP00000446466.1:p.Pro1050=
ENST00000578373.5:c.*2985C>A	ENSP00000463427.1:n.*2985C>A
ENST00000584450.5:c.3159+327C>A	ENSP00000463714.1:n.3159+327C>A
ENST00000584601.5:c.3105C>A	ENSP00000462438.1:p.Pro1035=
NM_001005862.2:c.3105C>A , LRG_724t1:c.3105C>A	NP_001005862.1:p.Pro1035=
NM_001289936.1:c.3150C>A , LRG_724t4:c.3150C>A	NP_001276865.1:p.Pro1050=
NM_001289937.1:c.3159+327C>A	NP_001276866.1:n.3159+327C>A
NM_004448.3:c.3195C>A , LRG_724t2:c.3195C>A	NP_004439.2:p.Pro1065=
NR_110535.1:n.3519C>A
XM_024450641.1:c.3333C>A	XP_024306409.1:p.Pro1111=
XM_024450642.1:c.3288C>A	XP_024306410.1:p.Pro1096=
XM_024450643.1:c.3243C>A	XP_024306411.1:p.Pro1081=
NM_001005862.3:c.3105C>A	NP_001005862.1:p.Pro1035=
NM_001289936.2:c.3150C>A	NP_001276865.1:p.Pro1050=
NM_001289937.2:c.3159+327C>A	NP_001276866.1:n.3159+327C>A
NM_001382782.1:c.3105C>A	NP_001369711.1:p.Pro1035=
NM_001382783.1:c.3105C>A	NP_001369712.1:p.Pro1035=
NM_001382784.1:c.3312C>A	NP_001369713.1:p.Pro1104=
NM_001382785.1:c.3297C>A	NP_001369714.1:p.Pro1099=
NM_001382786.1:c.3276C>A	NP_001369715.1:p.Pro1092=
NM_001382787.1:c.3270C>A	NP_001369716.1:p.Pro1090=
NM_001382788.1:c.3225C>A	NP_001369717.1:p.Pro1075=
NM_001382789.1:c.3216C>A	NP_001369718.1:p.Pro1072=
NM_001382790.1:c.3192C>A	NP_001369719.1:p.Pro1064=
NM_001382791.1:c.3186C>A	NP_001369720.1:p.Pro1062=
NM_001382792.1:c.3159C>A	NP_001369721.1:p.Pro1053=
NM_001382793.1:c.3153C>A	NP_001369722.1:p.Pro1051=
NM_001382794.1:c.3153C>A	NP_001369723.1:p.Pro1051=
NM_001382795.1:c.3147C>A	NP_001369724.1:p.Pro1049=
NM_001382796.1:c.3108C>A	NP_001369725.1:p.Pro1036=
NM_001382797.1:c.3096C>A	NP_001369726.1:p.Pro1032=
NM_001382798.1:c.3039C>A	NP_001369727.1:p.Pro1013=
NM_001382799.1:c.3015C>A	NP_001369728.1:p.Pro1005=
NM_001382800.1:c.3009C>A	NP_001369729.1:p.Pro1003=
NM_001382801.1:c.2991C>A	NP_001369730.1:p.Pro997=
NM_001382802.1:c.2937C>A	NP_001369731.1:p.Pro979=
NM_001382803.1:c.3117+327C>A	NP_001369732.1:n.3117+327C>A
NM_001382804.1:c.2367C>A	NP_001369733.1:p.Pro789=
NM_001382805.1:c.2244C>A	NP_001369734.1:p.Pro748=
NM_001382806.1:c.2157C>A	NP_001369735.1:p.Pro719=
NM_004448.4:c.3195C>A MANE Select	NP_004439.2:p.Pro1065=
NR_110535.2:n.3433C>A