Canonical Allele Identifier: CA399310830

Gene: ERBB2

Linked Data

• dbSNP Id: rs1294478912
• MyVariant Identifiers: chr17:g.37883685A>C (hg19) ; chr17:g.39727432A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727432A>C , CM000679.2:g.39727432A>C	GRCh38
NC_000017.10:g.37883685A>C , CM000679.1:g.37883685A>C	GRCh37
NC_000017.9:g.35137211A>C	NCBI36
NG_007503.1:g.44293A>C , LRG_724:g.44293A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3297A>C MANE Select	ENSP00000269571.4:p.Gln1099His
ENST00000269571.9:c.3297A>C	ENSP00000269571.4:p.Gln1099His
ENST00000406381.6:c.3207A>C	ENSP00000385185.2:p.Gln1069His
ENST00000445658.6:c.2469A>C	ENSP00000404047.2:p.Gln823His
ENST00000541774.5:c.3252A>C	ENSP00000446466.1:p.Gln1084His
ENST00000578373.5:c.*3087A>C	ENSP00000463427.1:n.*3087A>C
ENST00000584450.5:c.3160-257A>C	ENSP00000463714.1:n.3160-257A>C
ENST00000584601.5:c.3207A>C	ENSP00000462438.1:p.Gln1069His
NM_001005862.2:c.3207A>C , LRG_724t1:c.3207A>C	NP_001005862.1:p.Gln1069His
NM_001289936.1:c.3252A>C , LRG_724t4:c.3252A>C	NP_001276865.1:p.Gln1084His
NM_001289937.1:c.3160-257A>C	NP_001276866.1:n.3160-257A>C
NM_004448.3:c.3297A>C , LRG_724t2:c.3297A>C	NP_004439.2:p.Gln1099His
NR_110535.1:n.3621A>C
XM_024450641.1:c.3435A>C	XP_024306409.1:p.Gln1145His
XM_024450642.1:c.3390A>C	XP_024306410.1:p.Gln1130His
XM_024450643.1:c.3345A>C	XP_024306411.1:p.Gln1115His
NM_001005862.3:c.3207A>C	NP_001005862.1:p.Gln1069His
NM_001289936.2:c.3252A>C	NP_001276865.1:p.Gln1084His
NM_001289937.2:c.3160-257A>C	NP_001276866.1:n.3160-257A>C
NM_001382782.1:c.3207A>C	NP_001369711.1:p.Gln1069His
NM_001382783.1:c.3207A>C	NP_001369712.1:p.Gln1069His
NM_001382784.1:c.3414A>C	NP_001369713.1:p.Gln1138His
NM_001382785.1:c.3399A>C	NP_001369714.1:p.Gln1133His
NM_001382786.1:c.3378A>C	NP_001369715.1:p.Gln1126His
NM_001382787.1:c.3372A>C	NP_001369716.1:p.Gln1124His
NM_001382788.1:c.3327A>C	NP_001369717.1:p.Gln1109His
NM_001382789.1:c.3318A>C	NP_001369718.1:p.Gln1106His
NM_001382790.1:c.3294A>C	NP_001369719.1:p.Gln1098His
NM_001382791.1:c.3288A>C	NP_001369720.1:p.Gln1096His
NM_001382792.1:c.3261A>C	NP_001369721.1:p.Gln1087His
NM_001382793.1:c.3255A>C	NP_001369722.1:p.Gln1085His
NM_001382794.1:c.3255A>C	NP_001369723.1:p.Gln1085His
NM_001382795.1:c.3249A>C	NP_001369724.1:p.Gln1083His
NM_001382796.1:c.3210A>C	NP_001369725.1:p.Gln1070His
NM_001382797.1:c.3198A>C	NP_001369726.1:p.Gln1066His
NM_001382798.1:c.3141A>C	NP_001369727.1:p.Gln1047His
NM_001382799.1:c.3117A>C	NP_001369728.1:p.Gln1039His
NM_001382800.1:c.3111A>C	NP_001369729.1:p.Gln1037His
NM_001382801.1:c.3093A>C	NP_001369730.1:p.Gln1031His
NM_001382802.1:c.3039A>C	NP_001369731.1:p.Gln1013His
NM_001382803.1:c.3118-257A>C	NP_001369732.1:n.3118-257A>C
NM_001382804.1:c.2469A>C	NP_001369733.1:p.Gln823His
NM_001382805.1:c.2346A>C	NP_001369734.1:p.Gln782His
NM_001382806.1:c.2259A>C	NP_001369735.1:p.Gln753His
NM_004448.4:c.3297A>C MANE Select	NP_004439.2:p.Gln1099His
NR_110535.2:n.3535A>C