Canonical Allele Identifier: CA376557893

Gene: RET

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43123757T>C , CM000672.2:g.43123757T>C	GRCh38
NC_000010.10:g.43619205T>C , CM000672.1:g.43619205T>C	GRCh37
NC_000010.9:g.42939211T>C	NCBI36
NG_007489.1:g.51689T>C , LRG_518:g.51689T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_020975.6:c.2888T>C MANE Select	NP_066124.1:p.Leu963Pro
ENST00000355710.8:c.2888T>C MANE Select	ENSP00000347942.3:p.Leu963Pro
NM_001355216.1:c.2126T>C	NP_001342145.1:p.Leu709Pro
NM_020630.4:c.2888T>C , LRG_518t2:c.2888T>C	NP_065681.1:p.Leu963Pro
NM_020630.5:c.2888T>C	NP_065681.1:p.Leu963Pro
NM_020630.6:c.2888T>C	NP_065681.1:p.Leu963Pro
NM_020975.4:c.2888T>C , LRG_518t1:c.2888T>C	NP_066124.1:p.Leu963Pro
NM_020975.5:c.2888T>C	NP_066124.1:p.Leu963Pro
ENST00000340058.5:c.2888T>C	ENSP00000344798.4:p.Leu963Pro
ENST00000340058.6:c.2888T>C	ENSP00000344798.4:p.Leu963Pro
ENST00000355710.7:c.2888T>C	ENSP00000347942.3:p.Leu963Pro
ENST00000615310.4:c.*237T>C	ENSP00000480088.1:n.*237T>C
ENST00000615310.5:c.2492T>C	ENSP00000480088.2:p.Leu831Pro
ENST00000671844.1:c.*1482T>C	ENSP00000500541.1:n.*1482T>C
ENST00000672389.1:c.*1482T>C	ENSP00000500252.1:n.*1482T>C
ENST00000683007.1:n.2462T>C
XM_011540027.1:c.2888T>C	XP_011538329.1:p.Leu963Pro