Canonical Allele Identifier: CA2608875528

Gene: RET

Linked Data

• gnomAD v4: 10-43119493-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43119493T>A , CM000672.2:g.43119493T>A	GRCh38
NC_000010.10:g.43614941T>A , CM000672.1:g.43614941T>A	GRCh37
NC_000010.9:g.42934947T>A	NCBI36
NG_007489.1:g.47425T>A , LRG_518:g.47425T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.1997-38T>A	ENSP00000480088.2:n.1997-38T>A
ENST00000683007.1:n.1967-38T>A
ENST00000683872.1:n.1958-38T>A
ENST00000340058.6:c.2393-38T>A	ENSP00000344798.4:n.2393-38T>A
ENST00000355710.8:c.2393-38T>A MANE Select	ENSP00000347942.3:n.2393-38T>A
ENST00000671844.1:c.*987-38T>A	ENSP00000500541.1:n.*987-38T>A
ENST00000672389.1:c.*987-38T>A	ENSP00000500252.1:n.*987-38T>A
ENST00000340058.5:c.2393-38T>A	ENSP00000344798.4:n.2393-38T>A
ENST00000355710.7:c.2393-38T>A	ENSP00000347942.3:n.2393-38T>A
ENST00000615310.4:c.1290-209T>A	ENSP00000480088.1:n.1290-209T>A
NM_020630.4:c.2393-38T>A , LRG_518t2:c.2393-38T>A	NP_065681.1:n.2393-38T>A
NM_020975.4:c.2393-38T>A , LRG_518t1:c.2393-38T>A	NP_066124.1:n.2393-38T>A
XM_011540027.1:c.2393-38T>A	XP_011538329.1:n.2393-38T>A
NM_001355216.1:c.1631-38T>A	NP_001342145.1:n.1631-38T>A
NM_020630.5:c.2393-38T>A	NP_065681.1:n.2393-38T>A
NM_020975.5:c.2393-38T>A	NP_066124.1:n.2393-38T>A
NM_020975.6:c.2393-38T>A MANE Select	NP_066124.1:n.2393-38T>A
NM_020630.6:c.2393-38T>A	NP_065681.1:n.2393-38T>A