Canonical Allele Identifier: CA376552915

Gene: RET

Linked Data

• ClinVar Variation Id: 571671
• ClinVar RCV Id: RCV000692880
• dbSNP Id: rs776164321
• gnomAD v2: 10-43609952-G-T
• gnomAD v4: 10-43114504-G-T
• MyVariant Identifiers: chr10:g.43609952G>T (hg19) ; chr10:g.43114504G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43114504G>T , CM000672.2:g.43114504G>T	GRCh38
NC_000010.10:g.43609952G>T , CM000672.1:g.43609952G>T	GRCh37
NC_000010.9:g.42929958G>T	NCBI36
NG_007489.1:g.42436G>T , LRG_518:g.42436G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000615310.5:c.1508G>T	ENSP00000480088.2:p.Arg503Leu
ENST00000683007.1:n.1478G>T
ENST00000683872.1:n.1469G>T
ENST00000340058.6:c.1904G>T	ENSP00000344798.4:p.Arg635Leu
ENST00000355710.8:c.1904G>T MANE Select	ENSP00000347942.3:p.Arg635Leu
ENST00000671844.1:c.*498G>T	ENSP00000500541.1:n.*498G>T
ENST00000672389.1:c.*498G>T	ENSP00000500252.1:n.*498G>T
ENST00000340058.5:c.1904G>T	ENSP00000344798.4:p.Arg635Leu
ENST00000355710.7:c.1904G>T	ENSP00000347942.3:p.Arg635Leu
ENST00000498820.5:c.455G>T	ENSP00000419080.1:p.Arg152Leu
ENST00000615310.4:c.1289+3272G>T	ENSP00000480088.1:n.1289+3272G>T
NM_020630.4:c.1904G>T , LRG_518t2:c.1904G>T	NP_065681.1:p.Arg635Leu
NM_020975.4:c.1904G>T , LRG_518t1:c.1904G>T	NP_066124.1:p.Arg635Leu
XM_011540027.1:c.1904G>T	XP_011538329.1:p.Arg635Leu
NM_001355216.1:c.1142G>T	NP_001342145.1:p.Arg381Leu
NM_020630.5:c.1904G>T	NP_065681.1:p.Arg635Leu
NM_020975.5:c.1904G>T	NP_066124.1:p.Arg635Leu
NM_020975.6:c.1904G>T MANE Select	NP_066124.1:p.Arg635Leu
NM_020630.6:c.1904G>T	NP_065681.1:p.Arg635Leu