Canonical Allele Identifier: CA376550056

Gene: RET

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43111466G>A , CM000672.2:g.43111466G>A	GRCh38
NC_000010.10:g.43606914G>A , CM000672.1:g.43606914G>A	GRCh37
NC_000010.9:g.42926920G>A	NCBI36
NG_007489.1:g.39398G>A , LRG_518:g.39398G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_020975.6:c.1522+1G>A MANE Select	NP_066124.1:n.1522+1G>A
ENST00000355710.8:c.1522+1G>A MANE Select	ENSP00000347942.3:n.1522+1G>A
NM_001355216.1:c.760+1G>A	NP_001342145.1:n.760+1G>A
NM_020630.4:c.1522+1G>A , LRG_518t2:c.1522+1G>A	NP_065681.1:n.1522+1G>A
NM_020630.5:c.1522+1G>A	NP_065681.1:n.1522+1G>A
NM_020630.6:c.1522+1G>A	NP_065681.1:n.1522+1G>A
NM_020975.4:c.1522+1G>A , LRG_518t1:c.1522+1G>A	NP_066124.1:n.1522+1G>A
NM_020975.5:c.1522+1G>A	NP_066124.1:n.1522+1G>A
ENST00000340058.5:c.1522+1G>A	ENSP00000344798.4:n.1522+1G>A
ENST00000340058.6:c.1522+1G>A	ENSP00000344798.4:n.1522+1G>A
ENST00000355710.7:c.1522+1G>A	ENSP00000347942.3:n.1522+1G>A
ENST00000498820.5:c.74-633G>A	ENSP00000419080.1:n.74-633G>A
ENST00000615310.4:c.1289+234G>A	ENSP00000480088.1:n.1289+234G>A
ENST00000615310.5:c.1126+1G>A	ENSP00000480088.2:n.1126+1G>A
ENST00000671844.1:c.*116+1G>A	ENSP00000500541.1:n.*116+1G>A
ENST00000672389.1:c.*116+1G>A	ENSP00000500252.1:n.*116+1G>A
ENST00000683007.1:n.1096+1G>A
ENST00000683872.1:n.283+1G>A
XM_011540027.1:c.1522+1G>A	XP_011538329.1:n.1522+1G>A