Canonical Allele Identifier: CA2608894454

Gene: RET

Linked Data

• gnomAD v4: 10-43100751-G-GGCCCCCCCCCCCCCCC

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43100751_43100752insGCCCCCCCCCCCCCCC , CM000672.2:g.43100751_43100752insGCCCCCCCCCCCCCCC	GRCh38
NC_000010.10:g.43596199_43596200insGCCCCCCCCCCCCCCC , CM000672.1:g.43596199_43596200insGCCCCCCCCCCCCCCC	GRCh37
NC_000010.9:g.42916205_42916206insGCCCCCCCCCCCCCCC	NCBI36
NG_007489.1:g.28683_28684insGCCCCCCCCCCCCCCC , LRG_518:g.28683_28684insGCCCCCCCCCCCCCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.337+29_337+30insGCCCCCCCCCCCCCCC	ENSP00000480088.2:n.337+29_337+30insGCCCCCCCCCCCCCCC
ENST00000683278.1:c.239+29_239+30insGCCCCCCCCCCCCCCC
ENST00000684216.1:c.239+29_239+30insGCCCCCCCCCCCCCCC
ENST00000340058.6:c.337+29_337+30insGCCCCCCCCCCCCCCC	ENSP00000344798.4:n.337+29_337+30insGCCCCCCCCCCCCCCC
ENST00000355710.8:c.337+29_337+30insGCCCCCCCCCCCCCCC MANE Select	ENSP00000347942.3:n.337+29_337+30insGCCCCCCCCCCCCCCC
ENST00000638465.1:c.239+29_239+30insGCCCCCCCCCCCCCCC
ENST00000640619.1:c.239+29_239+30insGCCCCCCCCCCCCCCC
ENST00000671844.1:c.337+29_337+30insGCCCCCCCCCCCCCCC	ENSP00000500541.1:n.337+29_337+30insGCCCCCCCCCCCCCCC
ENST00000672389.1:c.74-10456_74-10455insGCCCCCCCCCCCCCCC	ENSP00000500252.1:n.74-10456_74-10455insGCCCCCCCCCCCCCCC
ENST00000340058.5:c.337+29_337+30insGCCCCCCCCCCCCCCC	ENSP00000344798.4:n.337+29_337+30insGCCCCCCCCCCCCCCC
ENST00000355710.7:c.337+29_337+30insGCCCCCCCCCCCCCCC	ENSP00000347942.3:n.337+29_337+30insGCCCCCCCCCCCCCCC
ENST00000498820.5:c.74-11348_74-11347insGCCCCCCCCCCCCCCC	ENSP00000419080.1:n.74-11348_74-11347insGCCCCCCCCCCCCCCC
ENST00000615310.4:c.337+29_337+30insGCCCCCCCCCCCCCCC	ENSP00000480088.1:n.337+29_337+30insGCCCCCCCCCCCCCCC
NM_020630.4:c.337+29_337+30insGCCCCCCCCCCCCCCC , LRG_518t2:c.337+29_337+30insGCCCCCCCCCCCCCCC	NP_065681.1:n.337+29_337+30insGCCCCCCCCCCCCCCC
NM_020975.4:c.337+29_337+30insGCCCCCCCCCCCCCCC , LRG_518t1:c.337+29_337+30insGCCCCCCCCCCCCCCC	NP_066124.1:n.337+29_337+30insGCCCCCCCCCCCCCCC
XM_011540027.1:c.337+29_337+30insGCCCCCCCCCCCCCCC	XP_011538329.1:n.337+29_337+30insGCCCCCCCCCCCCCCC
NM_020630.5:c.337+29_337+30insGCCCCCCCCCCCCCCC	NP_065681.1:n.337+29_337+30insGCCCCCCCCCCCCCCC
NM_020975.5:c.337+29_337+30insGCCCCCCCCCCCCCCC	NP_066124.1:n.337+29_337+30insGCCCCCCCCCCCCCCC
NM_020975.6:c.337+29_337+30insGCCCCCCCCCCCCCCC MANE Select	NP_066124.1:n.337+29_337+30insGCCCCCCCCCCCCCCC
NM_020630.6:c.337+29_337+30insGCCCCCCCCCCCCCCC	NP_065681.1:n.337+29_337+30insGCCCCCCCCCCCCCCC