Canonical Allele Identifier: CA376770894

Gene: RET

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43102471C>T , CM000672.2:g.43102471C>T	GRCh38
NC_000010.10:g.43597919C>T , CM000672.1:g.43597919C>T	GRCh37
NC_000010.9:g.42917925C>T	NCBI36
NG_007489.1:g.30403C>T , LRG_518:g.30403C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_020975.6:c.467C>T MANE Select	NP_066124.1:p.Ala156Val
ENST00000355710.8:c.467C>T MANE Select	ENSP00000347942.3:p.Ala156Val
NM_020630.4:c.467C>T , LRG_518t2:c.467C>T	NP_065681.1:p.Ala156Val
NM_020630.5:c.467C>T	NP_065681.1:p.Ala156Val
NM_020630.6:c.467C>T	NP_065681.1:p.Ala156Val
NM_020975.4:c.467C>T , LRG_518t1:c.467C>T	NP_066124.1:p.Ala156Val
NM_020975.5:c.467C>T	NP_066124.1:p.Ala156Val
ENST00000340058.5:c.467C>T	ENSP00000344798.4:p.Ala156Val
ENST00000340058.6:c.467C>T	ENSP00000344798.4:p.Ala156Val
ENST00000355710.7:c.467C>T	ENSP00000347942.3:p.Ala156Val
ENST00000498820.5:c.74-9628C>T	ENSP00000419080.1:n.74-9628C>T
ENST00000615310.4:c.467C>T	ENSP00000480088.1:p.Ala156Val
ENST00000615310.5:c.467C>T	ENSP00000480088.2:p.Ala156Val
ENST00000638465.1:c.409C>T
ENST00000640619.1:c.240C>T
ENST00000671844.1:c.467C>T	ENSP00000500541.1:p.Ala156Val
ENST00000672389.1:c.74-8736C>T	ENSP00000500252.1:n.74-8736C>T
ENST00000683278.1:c.388C>T
ENST00000684216.1:c.369C>T
XM_011540027.1:c.467C>T	XP_011538329.1:p.Ala156Val