Canonical Allele Identifier: CA1905836754

Gene: RET

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43100475C= , CM000672.2:g.43100475C=	GRCh38
NC_000010.10:g.43595923C= , CM000672.1:g.43595923C=	GRCh37
NC_000010.9:g.42915929C=	NCBI36
NG_007489.1:g.28407C= , LRG_518:g.28407C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.90C=	ENSP00000480088.2:p.Tyr30=
ENST00000340058.6:c.90C=	ENSP00000344798.4:p.Tyr30=
ENST00000355710.8:c.90C= MANE Select	ENSP00000347942.3:p.Tyr30=
ENST00000671844.1:c.90C=	ENSP00000500541.1:p.Tyr30=
ENST00000672389.1:c.74-10732C=	ENSP00000500252.1:n.74-10732C=
ENST00000340058.5:c.90C=	ENSP00000344798.4:p.Tyr30=
ENST00000355710.7:c.90C=	ENSP00000347942.3:p.Tyr30=
ENST00000498820.5:c.74-11624C=	ENSP00000419080.1:n.74-11624C=
ENST00000615310.4:c.90C=	ENSP00000480088.1:p.Tyr30=
NM_020630.4:c.90C= , LRG_518t2:c.90C=	NP_065681.1:p.Tyr30=
NM_020975.4:c.90C= , LRG_518t1:c.90C=	NP_066124.1:p.Tyr30=
XM_011540027.1:c.90C=	XP_011538329.1:p.Tyr30=
NM_020630.5:c.90C=	NP_065681.1:p.Tyr30=
NM_020975.5:c.90C=	NP_066124.1:p.Tyr30=
NM_020975.6:c.90C= MANE Select	NP_066124.1:p.Tyr30=
NM_020630.6:c.90C=	NP_065681.1:p.Tyr30=