Canonical Allele Identifier: CA376549771

Gene: RET

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43111410C>G , CM000672.2:g.43111410C>G	GRCh38
NC_000010.10:g.43606858C>G , CM000672.1:g.43606858C>G	GRCh37
NC_000010.9:g.42926864C>G	NCBI36
NG_007489.1:g.39342C>G , LRG_518:g.39342C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_020975.6:c.1467C>G MANE Select	NP_066124.1:p.Asp489Glu
ENST00000355710.8:c.1467C>G MANE Select	ENSP00000347942.3:p.Asp489Glu
NM_001355216.1:c.705C>G	NP_001342145.1:p.Asp235Glu
NM_020630.4:c.1467C>G , LRG_518t2:c.1467C>G	NP_065681.1:p.Asp489Glu
NM_020630.5:c.1467C>G	NP_065681.1:p.Asp489Glu
NM_020630.6:c.1467C>G	NP_065681.1:p.Asp489Glu
NM_020975.4:c.1467C>G , LRG_518t1:c.1467C>G	NP_066124.1:p.Asp489Glu
NM_020975.5:c.1467C>G	NP_066124.1:p.Asp489Glu
ENST00000340058.5:c.1467C>G	ENSP00000344798.4:p.Asp489Glu
ENST00000340058.6:c.1467C>G	ENSP00000344798.4:p.Asp489Glu
ENST00000355710.7:c.1467C>G	ENSP00000347942.3:p.Asp489Glu
ENST00000498820.5:c.74-689C>G	ENSP00000419080.1:n.74-689C>G
ENST00000615310.4:c.1289+178C>G	ENSP00000480088.1:n.1289+178C>G
ENST00000615310.5:c.1071C>G	ENSP00000480088.2:p.Asp357Glu
ENST00000671844.1:c.*61C>G	ENSP00000500541.1:n.*61C>G
ENST00000672389.1:c.*61C>G	ENSP00000500252.1:n.*61C>G
ENST00000683007.1:n.1041C>G
ENST00000683872.1:n.228C>G
XM_011540027.1:c.1467C>G	XP_011538329.1:p.Asp489Glu