Canonical Allele Identifier: CA469028954

Gene: RET

Linked Data

• dbSNP Id: rs2132963283
• MyVariant Identifiers: chr10:g.43615618T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43120170T>A , CM000672.2:g.43120170T>A	GRCh38
NC_000010.10:g.43615618T>A , CM000672.1:g.43615618T>A	GRCh37
NC_000010.9:g.42935624T>A	NCBI36
NG_007489.1:g.48102T>A , LRG_518:g.48102T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.2301T>A	ENSP00000480088.2:p.Val767=
ENST00000683007.1:n.2271T>A
ENST00000683872.1:n.2262T>A
ENST00000340058.6:c.2697T>A	ENSP00000344798.4:p.Val899=
ENST00000355710.8:c.2697T>A MANE Select	ENSP00000347942.3:p.Val899=
ENST00000671844.1:c.*1291T>A	ENSP00000500541.1:n.*1291T>A
ENST00000672389.1:c.*1291T>A	ENSP00000500252.1:n.*1291T>A
ENST00000340058.5:c.2697T>A	ENSP00000344798.4:p.Val899=
ENST00000355710.7:c.2697T>A	ENSP00000347942.3:p.Val899=
ENST00000615310.4:c.*46T>A	ENSP00000480088.1:n.*46T>A
NM_020630.4:c.2697T>A , LRG_518t2:c.2697T>A	NP_065681.1:p.Val899=
NM_020975.4:c.2697T>A , LRG_518t1:c.2697T>A	NP_066124.1:p.Val899=
XM_011540027.1:c.2697T>A	XP_011538329.1:p.Val899=
NM_001355216.1:c.1935T>A	NP_001342145.1:p.Val645=
NM_020630.5:c.2697T>A	NP_065681.1:p.Val899=
NM_020975.5:c.2697T>A	NP_066124.1:p.Val899=
NM_020975.6:c.2697T>A MANE Select	NP_066124.1:p.Val899=
NM_020630.6:c.2697T>A	NP_065681.1:p.Val899=