Canonical Allele Identifier: CA399313207

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143296369
• MyVariant Identifiers: chr17:g.37884038C>A (hg19) ; chr17:g.39727785C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727785C>A , CM000679.2:g.39727785C>A	GRCh38
NC_000017.10:g.37884038C>A , CM000679.1:g.37884038C>A	GRCh37
NC_000017.9:g.35137564C>A	NCBI36
NG_007503.1:g.44646C>A , LRG_724:g.44646C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3509C>A MANE Select	ENSP00000269571.4:p.Pro1170His
ENST00000269571.9:c.3509C>A	ENSP00000269571.4:p.Pro1170His
ENST00000406381.6:c.3419C>A	ENSP00000385185.2:p.Pro1140His
ENST00000445658.6:c.2681C>A	ENSP00000404047.2:p.Pro894His
ENST00000541774.5:c.3464C>A	ENSP00000446466.1:p.Pro1155His
ENST00000578373.5:c.*3299C>A	ENSP00000463427.1:n.*3299C>A
ENST00000584450.5:c.*88C>A	ENSP00000463714.1:n.*88C>A
ENST00000584601.5:c.3419C>A	ENSP00000462438.1:p.Pro1140His
NM_001005862.2:c.3419C>A , LRG_724t1:c.3419C>A	NP_001005862.1:p.Pro1140His
NM_001289936.1:c.3464C>A , LRG_724t4:c.3464C>A	NP_001276865.1:p.Pro1155His
NM_001289937.1:c.*88C>A	NP_001276866.1:n.*88C>A
NM_004448.3:c.3509C>A , LRG_724t2:c.3509C>A	NP_004439.2:p.Pro1170His
NR_110535.1:n.3833C>A
XM_024450641.1:c.3647C>A	XP_024306409.1:p.Pro1216His
XM_024450642.1:c.3602C>A	XP_024306410.1:p.Pro1201His
XM_024450643.1:c.3557C>A	XP_024306411.1:p.Pro1186His
NM_001005862.3:c.3419C>A	NP_001005862.1:p.Pro1140His
NM_001289936.2:c.3464C>A	NP_001276865.1:p.Pro1155His
NM_001289937.2:c.*88C>A	NP_001276866.1:n.*88C>A
NM_001382782.1:c.3419C>A	NP_001369711.1:p.Pro1140His
NM_001382783.1:c.3419C>A	NP_001369712.1:p.Pro1140His
NM_001382784.1:c.3626C>A	NP_001369713.1:p.Pro1209His
NM_001382785.1:c.3611C>A	NP_001369714.1:p.Pro1204His
NM_001382786.1:c.3590C>A	NP_001369715.1:p.Pro1197His
NM_001382787.1:c.3584C>A	NP_001369716.1:p.Pro1195His
NM_001382788.1:c.3539C>A	NP_001369717.1:p.Pro1180His
NM_001382789.1:c.3530C>A	NP_001369718.1:p.Pro1177His
NM_001382790.1:c.3506C>A	NP_001369719.1:p.Pro1169His
NM_001382791.1:c.3500C>A	NP_001369720.1:p.Pro1167His
NM_001382792.1:c.3473C>A	NP_001369721.1:p.Pro1158His
NM_001382793.1:c.3467C>A	NP_001369722.1:p.Pro1156His
NM_001382794.1:c.3467C>A	NP_001369723.1:p.Pro1156His
NM_001382795.1:c.3461C>A	NP_001369724.1:p.Pro1154His
NM_001382796.1:c.3422C>A	NP_001369725.1:p.Pro1141His
NM_001382797.1:c.3410C>A	NP_001369726.1:p.Pro1137His
NM_001382798.1:c.3353C>A	NP_001369727.1:p.Pro1118His
NM_001382799.1:c.3329C>A	NP_001369728.1:p.Pro1110His
NM_001382800.1:c.3323C>A	NP_001369729.1:p.Pro1108His
NM_001382801.1:c.3305C>A	NP_001369730.1:p.Pro1102His
NM_001382802.1:c.3251C>A	NP_001369731.1:p.Pro1084His
NM_001382803.1:c.*88C>A	NP_001369732.1:n.*88C>A
NM_001382804.1:c.2681C>A	NP_001369733.1:p.Pro894His
NM_001382805.1:c.2558C>A	NP_001369734.1:p.Pro853His
NM_001382806.1:c.2471C>A	NP_001369735.1:p.Pro824His
NM_004448.4:c.3509C>A MANE Select	NP_004439.2:p.Pro1170His
NR_110535.2:n.3747C>A