Canonical Allele Identifier: CA035935

Gene: RET

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43113674G>A , CM000672.2:g.43113674G>A	GRCh38
NC_000010.10:g.43609122G>A , CM000672.1:g.43609122G>A	GRCh37
NC_000010.9:g.42929128G>A	NCBI36
NG_007489.1:g.41606G>A , LRG_518:g.41606G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_020975.6:c.1878G>A MANE Select	NP_066124.1:p.Gln626=
ENST00000355710.8:c.1878G>A MANE Select	ENSP00000347942.3:p.Gln626=
NM_001355216.1:c.1116G>A	NP_001342145.1:p.Gln372=
NM_020630.4:c.1878G>A , LRG_518t2:c.1878G>A	NP_065681.1:p.Gln626=
NM_020630.5:c.1878G>A	NP_065681.1:p.Gln626=
NM_020630.6:c.1878G>A	NP_065681.1:p.Gln626=
NM_020975.4:c.1878G>A , LRG_518t1:c.1878G>A	NP_066124.1:p.Gln626=
NM_020975.5:c.1878G>A	NP_066124.1:p.Gln626=
ENST00000340058.5:c.1878G>A	ENSP00000344798.4:p.Gln626=
ENST00000340058.6:c.1878G>A	ENSP00000344798.4:p.Gln626=
ENST00000355710.7:c.1878G>A	ENSP00000347942.3:p.Gln626=
ENST00000498820.5:c.429G>A	ENSP00000419080.1:p.Gln143=
ENST00000615310.4:c.1289+2442G>A	ENSP00000480088.1:n.1289+2442G>A
ENST00000615310.5:c.1482G>A	ENSP00000480088.2:p.Gln494=
ENST00000671844.1:c.*472G>A	ENSP00000500541.1:n.*472G>A
ENST00000672389.1:c.*472G>A	ENSP00000500252.1:n.*472G>A
ENST00000683007.1:n.1452G>A
ENST00000683872.1:n.639G>A
XM_011540027.1:c.1878G>A	XP_011538329.1:p.Gln626=