Canonical Allele Identifier: CA2739265342

Gene: RET

Linked Data

• ClinVar Variation Id: 2812728
• ClinVar RCV Id: RCV003646263

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43119765C>A , CM000672.2:g.43119765C>A	GRCh38
NC_000010.10:g.43615213C>A , CM000672.1:g.43615213C>A	GRCh37
NC_000010.9:g.42935219C>A	NCBI36
NG_007489.1:g.47697C>A , LRG_518:g.47697C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.2211+20C>A	ENSP00000480088.2:n.2211+20C>A
ENST00000683007.1:n.2181+20C>A
ENST00000683872.1:n.2172+20C>A
ENST00000340058.6:c.2607+20C>A	ENSP00000344798.4:n.2607+20C>A
ENST00000355710.8:c.2607+20C>A MANE Select	ENSP00000347942.3:n.2607+20C>A
ENST00000671844.1:c.*1201+20C>A	ENSP00000500541.1:n.*1201+20C>A
ENST00000672389.1:c.*1201+20C>A	ENSP00000500252.1:n.*1201+20C>A
ENST00000340058.5:c.2607+20C>A	ENSP00000344798.4:n.2607+20C>A
ENST00000355710.7:c.2607+20C>A	ENSP00000347942.3:n.2607+20C>A
ENST00000615310.4:c.1333+20C>A	ENSP00000480088.1:n.1333+20C>A
NM_020630.4:c.2607+20C>A , LRG_518t2:c.2607+20C>A	NP_065681.1:n.2607+20C>A
NM_020975.4:c.2607+20C>A , LRG_518t1:c.2607+20C>A	NP_066124.1:n.2607+20C>A
XM_011540027.1:c.2607+20C>A	XP_011538329.1:n.2607+20C>A
NM_001355216.1:c.1845+20C>A	NP_001342145.1:n.1845+20C>A
NM_020630.5:c.2607+20C>A	NP_065681.1:n.2607+20C>A
NM_020975.5:c.2607+20C>A	NP_066124.1:n.2607+20C>A
NM_020975.6:c.2607+20C>A MANE Select	NP_066124.1:n.2607+20C>A
NM_020630.6:c.2607+20C>A	NP_065681.1:n.2607+20C>A