Canonical Allele Identifier: CA2787757068

Gene: RET

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43124814T>C , CM000672.2:g.43124814T>C	GRCh38
NC_000010.10:g.43620262T>C , CM000672.1:g.43620262T>C	GRCh37
NC_000010.9:g.42940268T>C	NCBI36
NG_007489.1:g.52746T>C , LRG_518:g.52746T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000615310.5:c.2544-69T>C	ENSP00000480088.2:n.2544-69T>C
ENST00000683007.1:n.2514-69T>C
ENST00000340058.6:c.2940-69T>C	ENSP00000344798.4:n.2940-69T>C
ENST00000355710.8:c.2940-69T>C MANE Select	ENSP00000347942.3:n.2940-69T>C
ENST00000671844.1:c.*1534-69T>C	ENSP00000500541.1:n.*1534-69T>C
ENST00000672389.1:c.*1534-69T>C	ENSP00000500252.1:n.*1534-69T>C
ENST00000340058.5:c.2940-69T>C	ENSP00000344798.4:n.2940-69T>C
ENST00000355710.7:c.2940-69T>C	ENSP00000347942.3:n.2940-69T>C
ENST00000615310.4:c.*289-69T>C	ENSP00000480088.1:n.*289-69T>C
NM_020630.4:c.2940-69T>C , LRG_518t2:c.2940-69T>C	NP_065681.1:n.2940-69T>C
NM_020975.4:c.2940-69T>C , LRG_518t1:c.2940-69T>C	NP_066124.1:n.2940-69T>C
XM_011540027.1:c.2940-69T>C	XP_011538329.1:n.2940-69T>C
NM_001355216.1:c.2178-69T>C	NP_001342145.1:n.2178-69T>C
NM_020630.5:c.2940-69T>C	NP_065681.1:n.2940-69T>C
NM_020975.5:c.2940-69T>C	NP_066124.1:n.2940-69T>C
NM_020975.6:c.2940-69T>C MANE Select	NP_066124.1:n.2940-69T>C
NM_020630.6:c.2940-69T>C	NP_065681.1:n.2940-69T>C