Canonical Allele Identifier: CA376770813

Gene: RET

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43102437G>A , CM000672.2:g.43102437G>A	GRCh38
NC_000010.10:g.43597885G>A , CM000672.1:g.43597885G>A	GRCh37
NC_000010.9:g.42917891G>A	NCBI36
NG_007489.1:g.30369G>A , LRG_518:g.30369G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_020975.6:c.433G>A MANE Select	NP_066124.1:p.Val145Ile
ENST00000355710.8:c.433G>A MANE Select	ENSP00000347942.3:p.Val145Ile
NM_020630.4:c.433G>A , LRG_518t2:c.433G>A	NP_065681.1:p.Val145Ile
NM_020630.5:c.433G>A	NP_065681.1:p.Val145Ile
NM_020630.6:c.433G>A	NP_065681.1:p.Val145Ile
NM_020975.4:c.433G>A , LRG_518t1:c.433G>A	NP_066124.1:p.Val145Ile
NM_020975.5:c.433G>A	NP_066124.1:p.Val145Ile
ENST00000340058.5:c.433G>A	ENSP00000344798.4:p.Val145Ile
ENST00000340058.6:c.433G>A	ENSP00000344798.4:p.Val145Ile
ENST00000355710.7:c.433G>A	ENSP00000347942.3:p.Val145Ile
ENST00000498820.5:c.74-9662G>A	ENSP00000419080.1:n.74-9662G>A
ENST00000615310.4:c.433G>A	ENSP00000480088.1:p.Val145Ile
ENST00000615310.5:c.433G>A	ENSP00000480088.2:p.Val145Ile
ENST00000638465.1:c.375G>A
ENST00000640619.1:c.240-34G>A
ENST00000671844.1:c.433G>A	ENSP00000500541.1:p.Val145Ile
ENST00000672389.1:c.74-8770G>A	ENSP00000500252.1:n.74-8770G>A
ENST00000683278.1:c.354G>A
ENST00000684216.1:c.335G>A
XM_011540027.1:c.433G>A	XP_011538329.1:p.Val145Ile