Canonical Allele Identifier: CA043594

Gene: RET

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43102402G>A , CM000672.2:g.43102402G>A	GRCh38
NC_000010.10:g.43597850G>A , CM000672.1:g.43597850G>A	GRCh37
NC_000010.9:g.42917856G>A	NCBI36
NG_007489.1:g.30334G>A , LRG_518:g.30334G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_020975.6:c.398G>A MANE Select	NP_066124.1:p.Arg133His
ENST00000355710.8:c.398G>A MANE Select	ENSP00000347942.3:p.Arg133His
NM_020630.4:c.398G>A , LRG_518t2:c.398G>A	NP_065681.1:p.Arg133His
NM_020630.5:c.398G>A	NP_065681.1:p.Arg133His
NM_020630.6:c.398G>A	NP_065681.1:p.Arg133His
NM_020975.4:c.398G>A , LRG_518t1:c.398G>A	NP_066124.1:p.Arg133His
NM_020975.5:c.398G>A	NP_066124.1:p.Arg133His
ENST00000340058.5:c.398G>A	ENSP00000344798.4:p.Arg133His
ENST00000340058.6:c.398G>A	ENSP00000344798.4:p.Arg133His
ENST00000355710.7:c.398G>A	ENSP00000347942.3:p.Arg133His
ENST00000498820.5:c.74-9697G>A	ENSP00000419080.1:n.74-9697G>A
ENST00000615310.4:c.398G>A	ENSP00000480088.1:p.Arg133His
ENST00000615310.5:c.398G>A	ENSP00000480088.2:p.Arg133His
ENST00000638465.1:c.340G>A
ENST00000640619.1:c.240-69G>A
ENST00000671844.1:c.398G>A	ENSP00000500541.1:p.Arg133His
ENST00000672389.1:c.74-8805G>A	ENSP00000500252.1:n.74-8805G>A
ENST00000683278.1:c.319G>A
ENST00000684216.1:c.300G>A
XM_011540027.1:c.398G>A	XP_011538329.1:p.Arg133His