Canonical Allele Identifier: CA376557165

Gene: RET

Linked Data

• dbSNP Id: rs2132961112
• MyVariant Identifiers: chr10:g.43615580A>T (hg19) ; chr10:g.43120132A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43120132A>T , CM000672.2:g.43120132A>T	GRCh38
NC_000010.10:g.43615580A>T , CM000672.1:g.43615580A>T	GRCh37
NC_000010.9:g.42935586A>T	NCBI36
NG_007489.1:g.48064A>T , LRG_518:g.48064A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000615310.5:c.2263A>T	ENSP00000480088.2:p.Lys755Ter
ENST00000683007.1:n.2233A>T
ENST00000683872.1:n.2224A>T
ENST00000340058.6:c.2659A>T	ENSP00000344798.4:p.Lys887Ter
ENST00000355710.8:c.2659A>T MANE Select	ENSP00000347942.3:p.Lys887Ter
ENST00000671844.1:c.*1253A>T	ENSP00000500541.1:n.*1253A>T
ENST00000672389.1:c.*1253A>T	ENSP00000500252.1:n.*1253A>T
ENST00000340058.5:c.2659A>T	ENSP00000344798.4:p.Lys887Ter
ENST00000355710.7:c.2659A>T	ENSP00000347942.3:p.Lys887Ter
ENST00000615310.4:c.*8A>T	ENSP00000480088.1:n.*8A>T
NM_020630.4:c.2659A>T , LRG_518t2:c.2659A>T	NP_065681.1:p.Lys887Ter
NM_020975.4:c.2659A>T , LRG_518t1:c.2659A>T	NP_066124.1:p.Lys887Ter
XM_011540027.1:c.2659A>T	XP_011538329.1:p.Lys887Ter
NM_001355216.1:c.1897A>T	NP_001342145.1:p.Lys633Ter
NM_020630.5:c.2659A>T	NP_065681.1:p.Lys887Ter
NM_020975.5:c.2659A>T	NP_066124.1:p.Lys887Ter
NM_020975.6:c.2659A>T MANE Select	NP_066124.1:p.Lys887Ter
NM_020630.6:c.2659A>T	NP_065681.1:p.Lys887Ter