Canonical Allele Identifier: CA399310737

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37883675A>T (hg19) ; chr17:g.39727422A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727422A>T , CM000679.2:g.39727422A>T	GRCh38
NC_000017.10:g.37883675A>T , CM000679.1:g.37883675A>T	GRCh37
NC_000017.9:g.35137201A>T	NCBI36
NG_007503.1:g.44283A>T , LRG_724:g.44283A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3287A>T MANE Select	ENSP00000269571.4:p.Lys1096Met
ENST00000269571.9:c.3287A>T	ENSP00000269571.4:p.Lys1096Met
ENST00000406381.6:c.3197A>T	ENSP00000385185.2:p.Lys1066Met
ENST00000445658.6:c.2459A>T	ENSP00000404047.2:p.Lys820Met
ENST00000541774.5:c.3242A>T	ENSP00000446466.1:p.Lys1081Met
ENST00000578373.5:c.*3077A>T	ENSP00000463427.1:n.*3077A>T
ENST00000584450.5:c.3160-267A>T	ENSP00000463714.1:n.3160-267A>T
ENST00000584601.5:c.3197A>T	ENSP00000462438.1:p.Lys1066Met
NM_001005862.2:c.3197A>T , LRG_724t1:c.3197A>T	NP_001005862.1:p.Lys1066Met
NM_001289936.1:c.3242A>T , LRG_724t4:c.3242A>T	NP_001276865.1:p.Lys1081Met
NM_001289937.1:c.3160-267A>T	NP_001276866.1:n.3160-267A>T
NM_004448.3:c.3287A>T , LRG_724t2:c.3287A>T	NP_004439.2:p.Lys1096Met
NR_110535.1:n.3611A>T
XM_024450641.1:c.3425A>T	XP_024306409.1:p.Lys1142Met
XM_024450642.1:c.3380A>T	XP_024306410.1:p.Lys1127Met
XM_024450643.1:c.3335A>T	XP_024306411.1:p.Lys1112Met
NM_001005862.3:c.3197A>T	NP_001005862.1:p.Lys1066Met
NM_001289936.2:c.3242A>T	NP_001276865.1:p.Lys1081Met
NM_001289937.2:c.3160-267A>T	NP_001276866.1:n.3160-267A>T
NM_001382782.1:c.3197A>T	NP_001369711.1:p.Lys1066Met
NM_001382783.1:c.3197A>T	NP_001369712.1:p.Lys1066Met
NM_001382784.1:c.3404A>T	NP_001369713.1:p.Lys1135Met
NM_001382785.1:c.3389A>T	NP_001369714.1:p.Lys1130Met
NM_001382786.1:c.3368A>T	NP_001369715.1:p.Lys1123Met
NM_001382787.1:c.3362A>T	NP_001369716.1:p.Lys1121Met
NM_001382788.1:c.3317A>T	NP_001369717.1:p.Lys1106Met
NM_001382789.1:c.3308A>T	NP_001369718.1:p.Lys1103Met
NM_001382790.1:c.3284A>T	NP_001369719.1:p.Lys1095Met
NM_001382791.1:c.3278A>T	NP_001369720.1:p.Lys1093Met
NM_001382792.1:c.3251A>T	NP_001369721.1:p.Lys1084Met
NM_001382793.1:c.3245A>T	NP_001369722.1:p.Lys1082Met
NM_001382794.1:c.3245A>T	NP_001369723.1:p.Lys1082Met
NM_001382795.1:c.3239A>T	NP_001369724.1:p.Lys1080Met
NM_001382796.1:c.3200A>T	NP_001369725.1:p.Lys1067Met
NM_001382797.1:c.3188A>T	NP_001369726.1:p.Lys1063Met
NM_001382798.1:c.3131A>T	NP_001369727.1:p.Lys1044Met
NM_001382799.1:c.3107A>T	NP_001369728.1:p.Lys1036Met
NM_001382800.1:c.3101A>T	NP_001369729.1:p.Lys1034Met
NM_001382801.1:c.3083A>T	NP_001369730.1:p.Lys1028Met
NM_001382802.1:c.3029A>T	NP_001369731.1:p.Lys1010Met
NM_001382803.1:c.3118-267A>T	NP_001369732.1:n.3118-267A>T
NM_001382804.1:c.2459A>T	NP_001369733.1:p.Lys820Met
NM_001382805.1:c.2336A>T	NP_001369734.1:p.Lys779Met
NM_001382806.1:c.2249A>T	NP_001369735.1:p.Lys750Met
NM_004448.4:c.3287A>T MANE Select	NP_004439.2:p.Lys1096Met
NR_110535.2:n.3525A>T