Canonical Allele Identifier: CA2787756161

Gene: RET

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43100791_43100797del , CM000672.2:g.43100791_43100797del	GRCh38
NC_000010.10:g.43596239_43596245del , CM000672.1:g.43596239_43596245del	GRCh37
NC_000010.9:g.42916245_42916251del	NCBI36
NG_007489.1:g.28723_28729del , LRG_518:g.28723_28729del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.337+69_337+75del	ENSP00000480088.2:n.337+69_337+75del
ENST00000683278.1:c.239+69_239+75del
ENST00000684216.1:c.239+69_239+75del
ENST00000340058.6:c.337+69_337+75del	ENSP00000344798.4:n.337+69_337+75del
ENST00000355710.8:c.337+69_337+75del MANE Select	ENSP00000347942.3:n.337+69_337+75del
ENST00000638465.1:c.239+69_239+75del
ENST00000640619.1:c.239+69_239+75del
ENST00000671844.1:c.337+69_337+75del	ENSP00000500541.1:n.337+69_337+75del
ENST00000672389.1:c.74-10416_74-10410del	ENSP00000500252.1:n.74-10416_74-10410del
ENST00000340058.5:c.337+69_337+75del	ENSP00000344798.4:n.337+69_337+75del
ENST00000355710.7:c.337+69_337+75del	ENSP00000347942.3:n.337+69_337+75del
ENST00000498820.5:c.74-11308_74-11302del	ENSP00000419080.1:n.74-11308_74-11302del
ENST00000615310.4:c.337+69_337+75del	ENSP00000480088.1:n.337+69_337+75del
NM_020630.4:c.337+69_337+75del , LRG_518t2:c.337+69_337+75del	NP_065681.1:n.337+69_337+75del
NM_020975.4:c.337+69_337+75del , LRG_518t1:c.337+69_337+75del	NP_066124.1:n.337+69_337+75del
XM_011540027.1:c.337+69_337+75del	XP_011538329.1:n.337+69_337+75del
NM_020630.5:c.337+69_337+75del	NP_065681.1:n.337+69_337+75del
NM_020975.5:c.337+69_337+75del	NP_066124.1:n.337+69_337+75del
NM_020975.6:c.337+69_337+75del MANE Select	NP_066124.1:n.337+69_337+75del
NM_020630.6:c.337+69_337+75del	NP_065681.1:n.337+69_337+75del