Canonical Allele Identifier: CA2608894501

Gene: RET

Linked Data

• gnomAD v4: 10-43100770-C-CAA

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43100770_43100771insAA , CM000672.2:g.43100770_43100771insAA	GRCh38
NC_000010.10:g.43596218_43596219insAA , CM000672.1:g.43596218_43596219insAA	GRCh37
NC_000010.9:g.42916224_42916225insAA	NCBI36
NG_007489.1:g.28702_28703insAA , LRG_518:g.28702_28703insAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.337+48_337+49insAA	ENSP00000480088.2:n.337+48_337+49insAA
ENST00000683278.1:c.239+48_239+49insAA
ENST00000684216.1:c.239+48_239+49insAA
ENST00000340058.6:c.337+48_337+49insAA	ENSP00000344798.4:n.337+48_337+49insAA
ENST00000355710.8:c.337+48_337+49insAA MANE Select	ENSP00000347942.3:n.337+48_337+49insAA
ENST00000638465.1:c.239+48_239+49insAA
ENST00000640619.1:c.239+48_239+49insAA
ENST00000671844.1:c.337+48_337+49insAA	ENSP00000500541.1:n.337+48_337+49insAA
ENST00000672389.1:c.74-10437_74-10436insAA	ENSP00000500252.1:n.74-10437_74-10436insAA
ENST00000340058.5:c.337+48_337+49insAA	ENSP00000344798.4:n.337+48_337+49insAA
ENST00000355710.7:c.337+48_337+49insAA	ENSP00000347942.3:n.337+48_337+49insAA
ENST00000498820.5:c.74-11329_74-11328insAA	ENSP00000419080.1:n.74-11329_74-11328insAA
ENST00000615310.4:c.337+48_337+49insAA	ENSP00000480088.1:n.337+48_337+49insAA
NM_020630.4:c.337+48_337+49insAA , LRG_518t2:c.337+48_337+49insAA	NP_065681.1:n.337+48_337+49insAA
NM_020975.4:c.337+48_337+49insAA , LRG_518t1:c.337+48_337+49insAA	NP_066124.1:n.337+48_337+49insAA
XM_011540027.1:c.337+48_337+49insAA	XP_011538329.1:n.337+48_337+49insAA
NM_020630.5:c.337+48_337+49insAA	NP_065681.1:n.337+48_337+49insAA
NM_020975.5:c.337+48_337+49insAA	NP_066124.1:n.337+48_337+49insAA
NM_020975.6:c.337+48_337+49insAA MANE Select	NP_066124.1:n.337+48_337+49insAA
NM_020630.6:c.337+48_337+49insAA	NP_065681.1:n.337+48_337+49insAA