Canonical Allele Identifier: CA2573053273

Gene: RET

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43122033C>T , CM000672.2:g.43122033C>T	GRCh38
NC_000010.10:g.43617481C>T , CM000672.1:g.43617481C>T	GRCh37
NC_000010.9:g.42937487C>T	NCBI36
NG_007489.1:g.49965C>T , LRG_518:g.49965C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_020975.6:c.2801+17C>T MANE Select	NP_066124.1:n.2801+17C>T
ENST00000355710.8:c.2801+17C>T MANE Select	ENSP00000347942.3:n.2801+17C>T
NM_001355216.1:c.2039+17C>T	NP_001342145.1:n.2039+17C>T
NM_020630.4:c.2801+17C>T , LRG_518t2:c.2801+17C>T	NP_065681.1:n.2801+17C>T
NM_020630.5:c.2801+17C>T	NP_065681.1:n.2801+17C>T
NM_020630.6:c.2801+17C>T	NP_065681.1:n.2801+17C>T
NM_020975.4:c.2801+17C>T , LRG_518t1:c.2801+17C>T	NP_066124.1:n.2801+17C>T
NM_020975.5:c.2801+17C>T	NP_066124.1:n.2801+17C>T
ENST00000340058.5:c.2801+17C>T	ENSP00000344798.4:n.2801+17C>T
ENST00000340058.6:c.2801+17C>T	ENSP00000344798.4:n.2801+17C>T
ENST00000355710.7:c.2801+17C>T	ENSP00000347942.3:n.2801+17C>T
ENST00000615310.4:c.*150+17C>T	ENSP00000480088.1:n.*150+17C>T
ENST00000615310.5:c.2405+17C>T	ENSP00000480088.2:n.2405+17C>T
ENST00000671844.1:c.*1395+17C>T	ENSP00000500541.1:n.*1395+17C>T
ENST00000672389.1:c.*1395+17C>T	ENSP00000500252.1:n.*1395+17C>T
ENST00000683007.1:n.2375+17C>T
XM_011540027.1:c.2801+17C>T	XP_011538329.1:n.2801+17C>T