Canonical Allele Identifier: CA376552761

Gene: RET

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43113624A>C , CM000672.2:g.43113624A>C	GRCh38
NC_000010.10:g.43609072A>C , CM000672.1:g.43609072A>C	GRCh37
NC_000010.9:g.42929078A>C	NCBI36
NG_007489.1:g.41556A>C , LRG_518:g.41556A>C

Transcript Alleles

HGVS	Amino-acid Change
NM_020975.6:c.1828A>C MANE Select	NP_066124.1:p.Asn610His
ENST00000355710.8:c.1828A>C MANE Select	ENSP00000347942.3:p.Asn610His
NM_001355216.1:c.1066A>C	NP_001342145.1:p.Asn356His
NM_020630.4:c.1828A>C , LRG_518t2:c.1828A>C	NP_065681.1:p.Asn610His
NM_020630.5:c.1828A>C	NP_065681.1:p.Asn610His
NM_020630.6:c.1828A>C	NP_065681.1:p.Asn610His
NM_020975.4:c.1828A>C , LRG_518t1:c.1828A>C	NP_066124.1:p.Asn610His
NM_020975.5:c.1828A>C	NP_066124.1:p.Asn610His
ENST00000340058.5:c.1828A>C	ENSP00000344798.4:p.Asn610His
ENST00000340058.6:c.1828A>C	ENSP00000344798.4:p.Asn610His
ENST00000355710.7:c.1828A>C	ENSP00000347942.3:p.Asn610His
ENST00000498820.5:c.379A>C	ENSP00000419080.1:p.Asn127His
ENST00000615310.4:c.1289+2392A>C	ENSP00000480088.1:n.1289+2392A>C
ENST00000615310.5:c.1432A>C	ENSP00000480088.2:p.Asn478His
ENST00000671844.1:c.*422A>C	ENSP00000500541.1:n.*422A>C
ENST00000672389.1:c.*422A>C	ENSP00000500252.1:n.*422A>C
ENST00000683007.1:n.1402A>C
ENST00000683872.1:n.589A>C
XM_011540027.1:c.1828A>C	XP_011538329.1:p.Asn610His