Canonical Allele Identifier: CA2697558301

Gene: RET

Linked Data

• ClinVar Variation Id: 2751049
• ClinVar RCV Id: RCV003531765
• dbSNP Id: rs2132666108

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43100741C>T , CM000672.2:g.43100741C>T	GRCh38
NC_000010.10:g.43596189C>T , CM000672.1:g.43596189C>T	GRCh37
NC_000010.9:g.42916195C>T	NCBI36
NG_007489.1:g.28673C>T , LRG_518:g.28673C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.337+19C>T	ENSP00000480088.2:n.337+19C>T
ENST00000683278.1:c.239+19C>T
ENST00000684216.1:c.239+19C>T
ENST00000340058.6:c.337+19C>T	ENSP00000344798.4:n.337+19C>T
ENST00000355710.8:c.337+19C>T MANE Select	ENSP00000347942.3:n.337+19C>T
ENST00000638465.1:c.239+19C>T
ENST00000640619.1:c.239+19C>T
ENST00000671844.1:c.337+19C>T	ENSP00000500541.1:n.337+19C>T
ENST00000672389.1:c.74-10466C>T	ENSP00000500252.1:n.74-10466C>T
ENST00000340058.5:c.337+19C>T	ENSP00000344798.4:n.337+19C>T
ENST00000355710.7:c.337+19C>T	ENSP00000347942.3:n.337+19C>T
ENST00000498820.5:c.74-11358C>T	ENSP00000419080.1:n.74-11358C>T
ENST00000615310.4:c.337+19C>T	ENSP00000480088.1:n.337+19C>T
NM_020630.4:c.337+19C>T , LRG_518t2:c.337+19C>T	NP_065681.1:n.337+19C>T
NM_020975.4:c.337+19C>T , LRG_518t1:c.337+19C>T	NP_066124.1:n.337+19C>T
XM_011540027.1:c.337+19C>T	XP_011538329.1:n.337+19C>T
NM_020630.5:c.337+19C>T	NP_065681.1:n.337+19C>T
NM_020975.5:c.337+19C>T	NP_066124.1:n.337+19C>T
NM_020975.6:c.337+19C>T MANE Select	NP_066124.1:n.337+19C>T
NM_020630.6:c.337+19C>T	NP_065681.1:n.337+19C>T