Canonical Allele Identifier: CA399310523

Gene: ERBB2

Linked Data

• dbSNP Id: rs200796676
• MyVariant Identifiers: chr17:g.37883638G>C (hg19) ; chr17:g.39727385G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727385G>C , CM000679.2:g.39727385G>C	GRCh38
NC_000017.10:g.37883638G>C , CM000679.1:g.37883638G>C	GRCh37
NC_000017.9:g.35137164G>C	NCBI36
NG_007503.1:g.44246G>C , LRG_724:g.44246G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3250G>C MANE Select	ENSP00000269571.4:p.Asp1084His
ENST00000269571.9:c.3250G>C	ENSP00000269571.4:p.Asp1084His
ENST00000406381.6:c.3160G>C	ENSP00000385185.2:p.Asp1054His
ENST00000445658.6:c.2422G>C	ENSP00000404047.2:p.Asp808His
ENST00000541774.5:c.3205G>C	ENSP00000446466.1:p.Asp1069His
ENST00000578373.5:c.*3040G>C	ENSP00000463427.1:n.*3040G>C
ENST00000584450.5:c.3160-304G>C	ENSP00000463714.1:n.3160-304G>C
ENST00000584601.5:c.3160G>C	ENSP00000462438.1:p.Asp1054His
NM_001005862.2:c.3160G>C , LRG_724t1:c.3160G>C	NP_001005862.1:p.Asp1054His
NM_001289936.1:c.3205G>C , LRG_724t4:c.3205G>C	NP_001276865.1:p.Asp1069His
NM_001289937.1:c.3160-304G>C	NP_001276866.1:n.3160-304G>C
NM_004448.3:c.3250G>C , LRG_724t2:c.3250G>C	NP_004439.2:p.Asp1084His
NR_110535.1:n.3574G>C
XM_024450641.1:c.3388G>C	XP_024306409.1:p.Asp1130His
XM_024450642.1:c.3343G>C	XP_024306410.1:p.Asp1115His
XM_024450643.1:c.3298G>C	XP_024306411.1:p.Asp1100His
NM_001005862.3:c.3160G>C	NP_001005862.1:p.Asp1054His
NM_001289936.2:c.3205G>C	NP_001276865.1:p.Asp1069His
NM_001289937.2:c.3160-304G>C	NP_001276866.1:n.3160-304G>C
NM_001382782.1:c.3160G>C	NP_001369711.1:p.Asp1054His
NM_001382783.1:c.3160G>C	NP_001369712.1:p.Asp1054His
NM_001382784.1:c.3367G>C	NP_001369713.1:p.Asp1123His
NM_001382785.1:c.3352G>C	NP_001369714.1:p.Asp1118His
NM_001382786.1:c.3331G>C	NP_001369715.1:p.Asp1111His
NM_001382787.1:c.3325G>C	NP_001369716.1:p.Asp1109His
NM_001382788.1:c.3280G>C	NP_001369717.1:p.Asp1094His
NM_001382789.1:c.3271G>C	NP_001369718.1:p.Asp1091His
NM_001382790.1:c.3247G>C	NP_001369719.1:p.Asp1083His
NM_001382791.1:c.3241G>C	NP_001369720.1:p.Asp1081His
NM_001382792.1:c.3214G>C	NP_001369721.1:p.Asp1072His
NM_001382793.1:c.3208G>C	NP_001369722.1:p.Asp1070His
NM_001382794.1:c.3208G>C	NP_001369723.1:p.Asp1070His
NM_001382795.1:c.3202G>C	NP_001369724.1:p.Asp1068His
NM_001382796.1:c.3163G>C	NP_001369725.1:p.Asp1055His
NM_001382797.1:c.3151G>C	NP_001369726.1:p.Asp1051His
NM_001382798.1:c.3094G>C	NP_001369727.1:p.Asp1032His
NM_001382799.1:c.3070G>C	NP_001369728.1:p.Asp1024His
NM_001382800.1:c.3064G>C	NP_001369729.1:p.Asp1022His
NM_001382801.1:c.3046G>C	NP_001369730.1:p.Asp1016His
NM_001382802.1:c.2992G>C	NP_001369731.1:p.Asp998His
NM_001382803.1:c.3118-304G>C	NP_001369732.1:n.3118-304G>C
NM_001382804.1:c.2422G>C	NP_001369733.1:p.Asp808His
NM_001382805.1:c.2299G>C	NP_001369734.1:p.Asp767His
NM_001382806.1:c.2212G>C	NP_001369735.1:p.Asp738His
NM_004448.4:c.3250G>C MANE Select	NP_004439.2:p.Asp1084His
NR_110535.2:n.3488G>C