Canonical Allele Identifier: CA376556859

Gene: RET

Linked Data

• dbSNP Id: rs2132951789
• MyVariant Identifiers: chr10:g.43615193G>A (hg19) ; chr10:g.43119745G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43119745G>A , CM000672.2:g.43119745G>A	GRCh38
NC_000010.10:g.43615193G>A , CM000672.1:g.43615193G>A	GRCh37
NC_000010.9:g.42935199G>A	NCBI36
NG_007489.1:g.47677G>A , LRG_518:g.47677G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.2211G>A	ENSP00000480088.2:p.Lys737=
ENST00000683007.1:n.2181G>A
ENST00000683872.1:n.2172G>A
ENST00000340058.6:c.2607G>A	ENSP00000344798.4:p.Lys869=
ENST00000355710.8:c.2607G>A MANE Select	ENSP00000347942.3:p.Lys869=
ENST00000671844.1:c.*1201G>A	ENSP00000500541.1:n.*1201G>A
ENST00000672389.1:c.*1201G>A	ENSP00000500252.1:n.*1201G>A
ENST00000340058.5:c.2607G>A	ENSP00000344798.4:p.Lys869=
ENST00000355710.7:c.2607G>A	ENSP00000347942.3:p.Lys869=
ENST00000615310.4:c.1333G>A	ENSP00000480088.1:p.Ala445Thr
NM_020630.4:c.2607G>A , LRG_518t2:c.2607G>A	NP_065681.1:p.Lys869=
NM_020975.4:c.2607G>A , LRG_518t1:c.2607G>A	NP_066124.1:p.Lys869=
XM_011540027.1:c.2607G>A	XP_011538329.1:p.Lys869=
NM_001355216.1:c.1845G>A	NP_001342145.1:p.Lys615=
NM_020630.5:c.2607G>A	NP_065681.1:p.Lys869=
NM_020975.5:c.2607G>A	NP_066124.1:p.Lys869=
NM_020975.6:c.2607G>A MANE Select	NP_066124.1:p.Lys869=
NM_020630.6:c.2607G>A	NP_065681.1:p.Lys869=