Canonical Allele Identifier: CA376553103

Gene: RET

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43114596A>T , CM000672.2:g.43114596A>T	GRCh38
NC_000010.10:g.43610044A>T , CM000672.1:g.43610044A>T	GRCh37
NC_000010.9:g.42930050A>T	NCBI36
NG_007489.1:g.42528A>T , LRG_518:g.42528A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.1600A>T	ENSP00000480088.2:p.Lys534Ter
ENST00000683007.1:n.1570A>T
ENST00000683872.1:n.1561A>T
ENST00000340058.6:c.1996A>T	ENSP00000344798.4:p.Lys666Ter
ENST00000355710.8:c.1996A>T MANE Select	ENSP00000347942.3:p.Lys666Ter
ENST00000671844.1:c.*590A>T	ENSP00000500541.1:n.*590A>T
ENST00000672389.1:c.*590A>T	ENSP00000500252.1:n.*590A>T
ENST00000340058.5:c.1996A>T	ENSP00000344798.4:p.Lys666Ter
ENST00000355710.7:c.1996A>T	ENSP00000347942.3:p.Lys666Ter
ENST00000615310.4:c.1289+3364A>T	ENSP00000480088.1:n.1289+3364A>T
NM_020630.4:c.1996A>T , LRG_518t2:c.1996A>T	NP_065681.1:p.Lys666Ter
NM_020975.4:c.1996A>T , LRG_518t1:c.1996A>T	NP_066124.1:p.Lys666Ter
XM_011540027.1:c.1996A>T	XP_011538329.1:p.Lys666Ter
NM_001355216.1:c.1234A>T	NP_001342145.1:p.Lys412Ter
NM_020630.5:c.1996A>T	NP_065681.1:p.Lys666Ter
NM_020975.5:c.1996A>T	NP_066124.1:p.Lys666Ter
NM_020975.6:c.1996A>T MANE Select	NP_066124.1:p.Lys666Ter
NM_020630.6:c.1996A>T	NP_065681.1:p.Lys666Ter