Canonical Allele Identifier: CA399304587

Gene: ERBB2

Linked Data

• dbSNP Id: rs2145865015
• MyVariant Identifiers: chr17:g.37881374C>A (hg19) ; chr17:g.39725121C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39725121C>A , CM000679.2:g.39725121C>A	GRCh38
NC_000017.10:g.37881374C>A , CM000679.1:g.37881374C>A	GRCh37
NC_000017.9:g.35134900C>A	NCBI36
NG_007503.1:g.41982C>A , LRG_724:g.41982C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2566C>A MANE Select	ENSP00000269571.4:p.Pro856Thr
ENST00000269571.9:c.2566C>A	ENSP00000269571.4:p.Pro856Thr
ENST00000406381.6:c.2476C>A	ENSP00000385185.2:p.Pro826Thr
ENST00000445658.6:c.1738C>A	ENSP00000404047.2:p.Pro580Thr
ENST00000541774.5:c.2521C>A	ENSP00000446466.1:p.Pro841Thr
ENST00000578373.5:c.*2356C>A	ENSP00000463427.1:n.*2356C>A
ENST00000580074.1:c.672C>A
ENST00000583038.5:n.3700C>A
ENST00000584450.5:c.2566C>A	ENSP00000463714.1:p.Pro856Thr
ENST00000584601.5:c.2476C>A	ENSP00000462438.1:p.Pro826Thr
NM_001005862.2:c.2476C>A , LRG_724t1:c.2476C>A	NP_001005862.1:p.Pro826Thr
NM_001289936.1:c.2521C>A , LRG_724t4:c.2521C>A	NP_001276865.1:p.Pro841Thr
NM_001289937.1:c.2566C>A	NP_001276866.1:p.Pro856Thr
NM_004448.3:c.2566C>A , LRG_724t2:c.2566C>A	NP_004439.2:p.Pro856Thr
NR_110535.1:n.2890C>A
XM_024450641.1:c.2704C>A	XP_024306409.1:p.Pro902Thr
XM_024450642.1:c.2659C>A	XP_024306410.1:p.Pro887Thr
XM_024450643.1:c.2614C>A	XP_024306411.1:p.Pro872Thr
NM_001005862.3:c.2476C>A	NP_001005862.1:p.Pro826Thr
NM_001289936.2:c.2521C>A	NP_001276865.1:p.Pro841Thr
NM_001289937.2:c.2566C>A	NP_001276866.1:p.Pro856Thr
NM_001382782.1:c.2476C>A	NP_001369711.1:p.Pro826Thr
NM_001382783.1:c.2476C>A	NP_001369712.1:p.Pro826Thr
NM_001382784.1:c.2683C>A	NP_001369713.1:p.Pro895Thr
NM_001382785.1:c.2668C>A	NP_001369714.1:p.Pro890Thr
NM_001382786.1:c.2647C>A	NP_001369715.1:p.Pro883Thr
NM_001382787.1:c.2641C>A	NP_001369716.1:p.Pro881Thr
NM_001382788.1:c.2596C>A	NP_001369717.1:p.Pro866Thr
NM_001382789.1:c.2587C>A	NP_001369718.1:p.Pro863Thr
NM_001382790.1:c.2563C>A	NP_001369719.1:p.Pro855Thr
NM_001382791.1:c.2557C>A	NP_001369720.1:p.Pro853Thr
NM_001382792.1:c.2530C>A	NP_001369721.1:p.Pro844Thr
NM_001382793.1:c.2524C>A	NP_001369722.1:p.Pro842Thr
NM_001382794.1:c.2524C>A	NP_001369723.1:p.Pro842Thr
NM_001382795.1:c.2518C>A	NP_001369724.1:p.Pro840Thr
NM_001382796.1:c.2566C>A	NP_001369725.1:p.Pro856Thr
NM_001382797.1:c.2467C>A	NP_001369726.1:p.Pro823Thr
NM_001382798.1:c.2494-206C>A	NP_001369727.1:n.2494-206C>A
NM_001382799.1:c.2386C>A	NP_001369728.1:p.Pro796Thr
NM_001382800.1:c.2380C>A	NP_001369729.1:p.Pro794Thr
NM_001382801.1:c.2446-206C>A	NP_001369730.1:n.2446-206C>A
NM_001382802.1:c.2308C>A	NP_001369731.1:p.Pro770Thr
NM_001382803.1:c.2524C>A	NP_001369732.1:p.Pro842Thr
NM_001382804.1:c.1738C>A	NP_001369733.1:p.Pro580Thr
NM_001382805.1:c.2208+1461C>A	NP_001369734.1:n.2208+1461C>A
NM_001382806.1:c.1528C>A	NP_001369735.1:p.Pro510Thr
NM_004448.4:c.2566C>A MANE Select	NP_004439.2:p.Pro856Thr
NR_110535.2:n.2804C>A