Canonical Allele Identifier: CA008212

Gene: RET

Linked Data

• dbSNP Id: rs121913308
• MyVariant Identifiers: chr10:g.43609940A>C (hg19) ; chr10:g.43114492A>C (hg38)
• PubMed: PMID:10049754

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43114492A>C , CM000672.2:g.43114492A>C	GRCh38
NC_000010.10:g.43609940A>C , CM000672.1:g.43609940A>C	GRCh37
NC_000010.9:g.42929946A>C	NCBI36
NG_007489.1:g.42424A>C , LRG_518:g.42424A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000615310.5:c.1496A>C	ENSP00000480088.2:p.Asp499Ala
ENST00000683007.1:n.1466A>C
ENST00000683872.1:n.1457A>C
ENST00000340058.6:c.1892A>C	ENSP00000344798.4:p.Asp631Ala
ENST00000355710.8:c.1892A>C MANE Select	ENSP00000347942.3:p.Asp631Ala
ENST00000671844.1:c.*486A>C	ENSP00000500541.1:n.*486A>C
ENST00000672389.1:c.*486A>C	ENSP00000500252.1:n.*486A>C
ENST00000340058.5:c.1892A>C	ENSP00000344798.4:p.Asp631Ala
ENST00000355710.7:c.1892A>C	ENSP00000347942.3:p.Asp631Ala
ENST00000498820.5:c.443A>C	ENSP00000419080.1:p.Asp148Ala
ENST00000615310.4:c.1289+3260A>C	ENSP00000480088.1:n.1289+3260A>C
NM_020630.4:c.1892A>C , LRG_518t2:c.1892A>C	NP_065681.1:p.Asp631Ala
NM_020975.4:c.1892A>C , LRG_518t1:c.1892A>C	NP_066124.1:p.Asp631Ala
XM_011540027.1:c.1892A>C	XP_011538329.1:p.Asp631Ala
NM_001355216.1:c.1130A>C	NP_001342145.1:p.Asp377Ala
NM_020630.5:c.1892A>C	NP_065681.1:p.Asp631Ala
NM_020975.5:c.1892A>C	NP_066124.1:p.Asp631Ala
NM_020975.6:c.1892A>C MANE Select	NP_066124.1:p.Asp631Ala
NM_020630.6:c.1892A>C	NP_065681.1:p.Asp631Ala