Canonical Allele Identifier: CA2608894496

Gene: RET

Linked Data

• gnomAD v4: 10-43100766-CCTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43100768_43100770del , CM000672.2:g.43100768_43100770del	GRCh38
NC_000010.10:g.43596216_43596218del , CM000672.1:g.43596216_43596218del	GRCh37
NC_000010.9:g.42916222_42916224del	NCBI36
NG_007489.1:g.28700_28702del , LRG_518:g.28700_28702del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.337+46_337+48del	ENSP00000480088.2:n.337+46_337+48del
ENST00000683278.1:c.239+46_239+48del
ENST00000684216.1:c.239+46_239+48del
ENST00000340058.6:c.337+46_337+48del	ENSP00000344798.4:n.337+46_337+48del
ENST00000355710.8:c.337+46_337+48del MANE Select	ENSP00000347942.3:n.337+46_337+48del
ENST00000638465.1:c.239+46_239+48del
ENST00000640619.1:c.239+46_239+48del
ENST00000671844.1:c.337+46_337+48del	ENSP00000500541.1:n.337+46_337+48del
ENST00000672389.1:c.74-10439_74-10437del	ENSP00000500252.1:n.74-10439_74-10437del
ENST00000340058.5:c.337+46_337+48del	ENSP00000344798.4:n.337+46_337+48del
ENST00000355710.7:c.337+46_337+48del	ENSP00000347942.3:n.337+46_337+48del
ENST00000498820.5:c.74-11331_74-11329del	ENSP00000419080.1:n.74-11331_74-11329del
ENST00000615310.4:c.337+46_337+48del	ENSP00000480088.1:n.337+46_337+48del
NM_020630.4:c.337+46_337+48del , LRG_518t2:c.337+46_337+48del	NP_065681.1:n.337+46_337+48del
NM_020975.4:c.337+46_337+48del , LRG_518t1:c.337+46_337+48del	NP_066124.1:n.337+46_337+48del
XM_011540027.1:c.337+46_337+48del	XP_011538329.1:n.337+46_337+48del
NM_020630.5:c.337+46_337+48del	NP_065681.1:n.337+46_337+48del
NM_020975.5:c.337+46_337+48del	NP_066124.1:n.337+46_337+48del
NM_020975.6:c.337+46_337+48del MANE Select	NP_066124.1:n.337+46_337+48del
NM_020630.6:c.337+46_337+48del	NP_065681.1:n.337+46_337+48del