Canonical Allele Identifier: CA376557250

Gene: RET

Linked Data

• ClinVar Variation Id: 3008967
• ClinVar RCV Id: RCV003862094
• MyVariant Identifiers: chr10:g.43615620A>C (hg19) ; chr10:g.43120172A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43120172A>C , CM000672.2:g.43120172A>C	GRCh38
NC_000010.10:g.43615620A>C , CM000672.1:g.43615620A>C	GRCh37
NC_000010.9:g.42935626A>C	NCBI36
NG_007489.1:g.48104A>C , LRG_518:g.48104A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.2303A>C	ENSP00000480088.2:p.Tyr768Ser
ENST00000683007.1:n.2273A>C
ENST00000683872.1:n.2264A>C
ENST00000340058.6:c.2699A>C	ENSP00000344798.4:p.Tyr900Ser
ENST00000355710.8:c.2699A>C MANE Select	ENSP00000347942.3:p.Tyr900Ser
ENST00000671844.1:c.*1293A>C	ENSP00000500541.1:n.*1293A>C
ENST00000672389.1:c.*1293A>C	ENSP00000500252.1:n.*1293A>C
ENST00000340058.5:c.2699A>C	ENSP00000344798.4:p.Tyr900Ser
ENST00000355710.7:c.2699A>C	ENSP00000347942.3:p.Tyr900Ser
ENST00000615310.4:c.*48A>C	ENSP00000480088.1:n.*48A>C
NM_020630.4:c.2699A>C , LRG_518t2:c.2699A>C	NP_065681.1:p.Tyr900Ser
NM_020975.4:c.2699A>C , LRG_518t1:c.2699A>C	NP_066124.1:p.Tyr900Ser
XM_011540027.1:c.2699A>C	XP_011538329.1:p.Tyr900Ser
NM_001355216.1:c.1937A>C	NP_001342145.1:p.Tyr646Ser
NM_020630.5:c.2699A>C	NP_065681.1:p.Tyr900Ser
NM_020975.5:c.2699A>C	NP_066124.1:p.Tyr900Ser
NM_020975.6:c.2699A>C MANE Select	NP_066124.1:p.Tyr900Ser
NM_020630.6:c.2699A>C	NP_065681.1:p.Tyr900Ser