Canonical Allele Identifier: CA376545666

Gene: RET

Linked Data

• MyVariant Identifiers: chr10:g.43601837C>A (hg19) ; chr10:g.43106389C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43106389C>A , CM000672.2:g.43106389C>A	GRCh38
NC_000010.10:g.43601837C>A , CM000672.1:g.43601837C>A	GRCh37
NC_000010.9:g.42921843C>A	NCBI36
NG_007489.1:g.34321C>A , LRG_518:g.34321C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000615310.5:c.867+1196C>A	ENSP00000480088.2:n.867+1196C>A
ENST00000683007.1:n.455C>A
ENST00000340058.6:c.881C>A	ENSP00000344798.4:p.Ala294Asp
ENST00000355710.8:c.881C>A MANE Select	ENSP00000347942.3:p.Ala294Asp
ENST00000671844.1:c.625+3760C>A	ENSP00000500541.1:n.625+3760C>A
ENST00000672389.1:c.74-4818C>A	ENSP00000500252.1:n.74-4818C>A
ENST00000340058.5:c.881C>A	ENSP00000344798.4:p.Ala294Asp
ENST00000355710.7:c.881C>A	ENSP00000347942.3:p.Ala294Asp
ENST00000479913.1:n.476C>A
ENST00000498820.5:c.74-5710C>A	ENSP00000419080.1:n.74-5710C>A
ENST00000615310.4:c.881C>A	ENSP00000480088.1:p.Ala294Asp
NM_020630.4:c.881C>A , LRG_518t2:c.881C>A	NP_065681.1:p.Ala294Asp
NM_020975.4:c.881C>A , LRG_518t1:c.881C>A	NP_066124.1:p.Ala294Asp
XM_011540027.1:c.881C>A	XP_011538329.1:p.Ala294Asp
NM_001355216.1:c.119C>A	NP_001342145.1:p.Ala40Asp
NM_020630.5:c.881C>A	NP_065681.1:p.Ala294Asp
NM_020975.5:c.881C>A	NP_066124.1:p.Ala294Asp
NM_020975.6:c.881C>A MANE Select	NP_066124.1:p.Ala294Asp
NM_020630.6:c.881C>A	NP_065681.1:p.Ala294Asp