Canonical Allele Identifier: CA1905819661

Gene: RET

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43119896T= , CM000672.2:g.43119896T=	GRCh38
NC_000010.10:g.43615344T= , CM000672.1:g.43615344T=	GRCh37
NC_000010.9:g.42935350T=	NCBI36
NG_007489.1:g.47828T= , LRG_518:g.47828T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.2211+151T=	ENSP00000480088.2:n.2211+151T=
ENST00000683007.1:n.2181+151T=
ENST00000683872.1:n.2172+151T=
ENST00000340058.6:c.2607+151T=	ENSP00000344798.4:n.2607+151T=
ENST00000355710.8:c.2607+151T= MANE Select	ENSP00000347942.3:n.2607+151T=
ENST00000671844.1:c.*1201+151T=	ENSP00000500541.1:n.*1201+151T=
ENST00000672389.1:c.*1201+151T=	ENSP00000500252.1:n.*1201+151T=
ENST00000340058.5:c.2607+151T=	ENSP00000344798.4:n.2607+151T=
ENST00000355710.7:c.2607+151T=	ENSP00000347942.3:n.2607+151T=
ENST00000615310.4:c.1333+151T=	ENSP00000480088.1:n.1333+151T=
NM_020630.4:c.2607+151T= , LRG_518t2:c.2607+151T=	NP_065681.1:n.2607+151T=
NM_020975.4:c.2607+151T= , LRG_518t1:c.2607+151T=	NP_066124.1:n.2607+151T=
XM_011540027.1:c.2607+151T=	XP_011538329.1:n.2607+151T=
NM_001355216.1:c.1845+151T=	NP_001342145.1:n.1845+151T=
NM_020630.5:c.2607+151T=	NP_065681.1:n.2607+151T=
NM_020975.5:c.2607+151T=	NP_066124.1:n.2607+151T=
NM_020975.6:c.2607+151T= MANE Select	NP_066124.1:n.2607+151T=
NM_020630.6:c.2607+151T=	NP_065681.1:n.2607+151T=