Canonical Allele Identifier: CA2608894460

Gene: RET

Linked Data

• gnomAD v4: 10-43100753-G-GGCCCCCCCCCCCCCCCC

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43100753_43100754insGCCCCCCCCCCCCCCCC , CM000672.2:g.43100753_43100754insGCCCCCCCCCCCCCCCC	GRCh38
NC_000010.10:g.43596201_43596202insGCCCCCCCCCCCCCCCC , CM000672.1:g.43596201_43596202insGCCCCCCCCCCCCCCCC	GRCh37
NC_000010.9:g.42916207_42916208insGCCCCCCCCCCCCCCCC	NCBI36
NG_007489.1:g.28685_28686insGCCCCCCCCCCCCCCCC , LRG_518:g.28685_28686insGCCCCCCCCCCCCCCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.337+31_337+32insGCCCCCCCCCCCCCCCC	ENSP00000480088.2:n.337+31_337+32insGCCCCCCCCCCCCCCCC
ENST00000683278.1:c.239+31_239+32insGCCCCCCCCCCCCCCCC
ENST00000684216.1:c.239+31_239+32insGCCCCCCCCCCCCCCCC
ENST00000340058.6:c.337+31_337+32insGCCCCCCCCCCCCCCCC	ENSP00000344798.4:n.337+31_337+32insGCCCCCCCCCCCCCCCC
ENST00000355710.8:c.337+31_337+32insGCCCCCCCCCCCCCCCC MANE Select	ENSP00000347942.3:n.337+31_337+32insGCCCCCCCCCCCCCCCC
ENST00000638465.1:c.239+31_239+32insGCCCCCCCCCCCCCCCC
ENST00000640619.1:c.239+31_239+32insGCCCCCCCCCCCCCCCC
ENST00000671844.1:c.337+31_337+32insGCCCCCCCCCCCCCCCC	ENSP00000500541.1:n.337+31_337+32insGCCCCCCCCCCCCCCCC
ENST00000672389.1:c.74-10454_74-10453insGCCCCCCCCCCCCCCCC	ENSP00000500252.1:n.74-10454_74-10453insGCCCCCCCCCCCCCCCC
ENST00000340058.5:c.337+31_337+32insGCCCCCCCCCCCCCCCC	ENSP00000344798.4:n.337+31_337+32insGCCCCCCCCCCCCCCCC
ENST00000355710.7:c.337+31_337+32insGCCCCCCCCCCCCCCCC	ENSP00000347942.3:n.337+31_337+32insGCCCCCCCCCCCCCCCC
ENST00000498820.5:c.74-11346_74-11345insGCCCCCCCCCCCCCCCC	ENSP00000419080.1:n.74-11346_74-11345insGCCCCCCCCCCCCCCCC
ENST00000615310.4:c.337+31_337+32insGCCCCCCCCCCCCCCCC	ENSP00000480088.1:n.337+31_337+32insGCCCCCCCCCCCCCCCC
NM_020630.4:c.337+31_337+32insGCCCCCCCCCCCCCCCC , LRG_518t2:c.337+31_337+32insGCCCCCCCCCCCCCCCC	NP_065681.1:n.337+31_337+32insGCCCCCCCCCCCCCCCC
NM_020975.4:c.337+31_337+32insGCCCCCCCCCCCCCCCC , LRG_518t1:c.337+31_337+32insGCCCCCCCCCCCCCCCC	NP_066124.1:n.337+31_337+32insGCCCCCCCCCCCCCCCC
XM_011540027.1:c.337+31_337+32insGCCCCCCCCCCCCCCCC	XP_011538329.1:n.337+31_337+32insGCCCCCCCCCCCCCCCC
NM_020630.5:c.337+31_337+32insGCCCCCCCCCCCCCCCC	NP_065681.1:n.337+31_337+32insGCCCCCCCCCCCCCCCC
NM_020975.5:c.337+31_337+32insGCCCCCCCCCCCCCCCC	NP_066124.1:n.337+31_337+32insGCCCCCCCCCCCCCCCC
NM_020975.6:c.337+31_337+32insGCCCCCCCCCCCCCCCC MANE Select	NP_066124.1:n.337+31_337+32insGCCCCCCCCCCCCCCCC
NM_020630.6:c.337+31_337+32insGCCCCCCCCCCCCCCCC	NP_065681.1:n.337+31_337+32insGCCCCCCCCCCCCCCCC