Canonical Allele Identifier: CA1905836786

Gene: RET

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43100538G= , CM000672.2:g.43100538G=	GRCh38
NC_000010.10:g.43595986G= , CM000672.1:g.43595986G=	GRCh37
NC_000010.9:g.42915992G=	NCBI36
NG_007489.1:g.28470G= , LRG_518:g.28470G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.153G=	ENSP00000480088.2:p.Leu51=
ENST00000683278.1:c.55G=
ENST00000684216.1:c.55G=
ENST00000340058.6:c.153G=	ENSP00000344798.4:p.Leu51=
ENST00000355710.8:c.153G= MANE Select	ENSP00000347942.3:p.Leu51=
ENST00000638465.1:c.55G=
ENST00000640619.1:c.55G=
ENST00000671844.1:c.153G=	ENSP00000500541.1:p.Leu51=
ENST00000672389.1:c.74-10669G=	ENSP00000500252.1:n.74-10669G=
ENST00000340058.5:c.153G=	ENSP00000344798.4:p.Leu51=
ENST00000355710.7:c.153G=	ENSP00000347942.3:p.Leu51=
ENST00000498820.5:c.74-11561G=	ENSP00000419080.1:n.74-11561G=
ENST00000615310.4:c.153G=	ENSP00000480088.1:p.Leu51=
NM_020630.4:c.153G= , LRG_518t2:c.153G=	NP_065681.1:p.Leu51=
NM_020975.4:c.153G= , LRG_518t1:c.153G=	NP_066124.1:p.Leu51=
XM_011540027.1:c.153G=	XP_011538329.1:p.Leu51=
NM_020630.5:c.153G=	NP_065681.1:p.Leu51=
NM_020975.5:c.153G=	NP_066124.1:p.Leu51=
NM_020975.6:c.153G= MANE Select	NP_066124.1:p.Leu51=
NM_020630.6:c.153G=	NP_065681.1:p.Leu51=