Canonical Allele Identifier: CA1905836873

Gene: RET

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43100720G= , CM000672.2:g.43100720G=	GRCh38
NC_000010.10:g.43596168G= , CM000672.1:g.43596168G=	GRCh37
NC_000010.9:g.42916174G=	NCBI36
NG_007489.1:g.28652G= , LRG_518:g.28652G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.335G=	ENSP00000480088.2:p.Arg112=
ENST00000683278.1:c.237G=
ENST00000684216.1:c.237G=
ENST00000340058.6:c.335G=	ENSP00000344798.4:p.Arg112=
ENST00000355710.8:c.335G= MANE Select	ENSP00000347942.3:p.Arg112=
ENST00000638465.1:c.237G=
ENST00000640619.1:c.237G=
ENST00000671844.1:c.335G=	ENSP00000500541.1:p.Arg112=
ENST00000672389.1:c.74-10487G=	ENSP00000500252.1:n.74-10487G=
ENST00000340058.5:c.335G=	ENSP00000344798.4:p.Arg112=
ENST00000355710.7:c.335G=	ENSP00000347942.3:p.Arg112=
ENST00000498820.5:c.74-11379G=	ENSP00000419080.1:n.74-11379G=
ENST00000615310.4:c.335G=	ENSP00000480088.1:p.Arg112=
NM_020630.4:c.335G= , LRG_518t2:c.335G=	NP_065681.1:p.Arg112=
NM_020975.4:c.335G= , LRG_518t1:c.335G=	NP_066124.1:p.Arg112=
XM_011540027.1:c.335G=	XP_011538329.1:p.Arg112=
NM_020630.5:c.335G=	NP_065681.1:p.Arg112=
NM_020975.5:c.335G=	NP_066124.1:p.Arg112=
NM_020975.6:c.335G= MANE Select	NP_066124.1:p.Arg112=
NM_020630.6:c.335G=	NP_065681.1:p.Arg112=