Canonical Allele Identifier: CA1905819564

Gene: RET

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43119810_43119812delinsCTG , CM000672.2:g.43119810_43119812delinsCTG	GRCh38
NC_000010.10:g.43615258_43615260delinsCTG , CM000672.1:g.43615258_43615260delinsCTG	GRCh37
NC_000010.9:g.42935264_42935266delinsCTG	NCBI36
NG_007489.1:g.47742_47744delinsCTG , LRG_518:g.47742_47744delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.2211+65_2211+67delinsCTG	ENSP00000480088.2:n.2211+65_2211+67delinsCTG
ENST00000683007.1:n.2181+65_2181+67delinsCTG
ENST00000683872.1:n.2172+65_2172+67delinsCTG
ENST00000340058.6:c.2607+65_2607+67delinsCTG	ENSP00000344798.4:n.2607+65_2607+67delinsCTG
ENST00000355710.8:c.2607+65_2607+67delinsCTG MANE Select	ENSP00000347942.3:n.2607+65_2607+67delinsCTG
ENST00000671844.1:c.*1201+65_*1201+67delinsCTG	ENSP00000500541.1:n.*1201+65_*1201+67delinsCTG
ENST00000672389.1:c.*1201+65_*1201+67delinsCTG	ENSP00000500252.1:n.*1201+65_*1201+67delinsCTG
ENST00000340058.5:c.2607+65_2607+67delinsCTG	ENSP00000344798.4:n.2607+65_2607+67delinsCTG
ENST00000355710.7:c.2607+65_2607+67delinsCTG	ENSP00000347942.3:n.2607+65_2607+67delinsCTG
ENST00000615310.4:c.1333+65_1333+67delinsCTG	ENSP00000480088.1:n.1333+65_1333+67delinsCTG
NM_020630.4:c.2607+65_2607+67delinsCTG , LRG_518t2:c.2607+65_2607+67delinsCTG	NP_065681.1:n.2607+65_2607+67delinsCTG
NM_020975.4:c.2607+65_2607+67delinsCTG , LRG_518t1:c.2607+65_2607+67delinsCTG	NP_066124.1:n.2607+65_2607+67delinsCTG
XM_011540027.1:c.2607+65_2607+67delinsCTG	XP_011538329.1:n.2607+65_2607+67delinsCTG
NM_001355216.1:c.1845+65_1845+67delinsCTG	NP_001342145.1:n.1845+65_1845+67delinsCTG
NM_020630.5:c.2607+65_2607+67delinsCTG	NP_065681.1:n.2607+65_2607+67delinsCTG
NM_020975.5:c.2607+65_2607+67delinsCTG	NP_066124.1:n.2607+65_2607+67delinsCTG
NM_020975.6:c.2607+65_2607+67delinsCTG MANE Select	NP_066124.1:n.2607+65_2607+67delinsCTG
NM_020630.6:c.2607+65_2607+67delinsCTG	NP_065681.1:n.2607+65_2607+67delinsCTG