Canonical Allele Identifier: CA376556672

Gene: RET

Linked Data

• ClinVar Variation Id: 2868475
• ClinVar RCV Id: RCV003646756
• MyVariant Identifiers: chr10:g.43615159T>C (hg19) ; chr10:g.43119711T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43119711T>C , CM000672.2:g.43119711T>C	GRCh38
NC_000010.10:g.43615159T>C , CM000672.1:g.43615159T>C	GRCh37
NC_000010.9:g.42935165T>C	NCBI36
NG_007489.1:g.47643T>C , LRG_518:g.47643T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.2177T>C	ENSP00000480088.2:p.Ile726Thr
ENST00000683007.1:n.2147T>C
ENST00000683872.1:n.2138T>C
ENST00000340058.6:c.2573T>C	ENSP00000344798.4:p.Ile858Thr
ENST00000355710.8:c.2573T>C MANE Select	ENSP00000347942.3:p.Ile858Thr
ENST00000671844.1:c.*1167T>C	ENSP00000500541.1:n.*1167T>C
ENST00000672389.1:c.*1167T>C	ENSP00000500252.1:n.*1167T>C
ENST00000340058.5:c.2573T>C	ENSP00000344798.4:p.Ile858Thr
ENST00000355710.7:c.2573T>C	ENSP00000347942.3:p.Ile858Thr
ENST00000615310.4:c.1299T>C	ENSP00000480088.1:p.Asp433=
NM_020630.4:c.2573T>C , LRG_518t2:c.2573T>C	NP_065681.1:p.Ile858Thr
NM_020975.4:c.2573T>C , LRG_518t1:c.2573T>C	NP_066124.1:p.Ile858Thr
XM_011540027.1:c.2573T>C	XP_011538329.1:p.Ile858Thr
NM_001355216.1:c.1811T>C	NP_001342145.1:p.Ile604Thr
NM_020630.5:c.2573T>C	NP_065681.1:p.Ile858Thr
NM_020975.5:c.2573T>C	NP_066124.1:p.Ile858Thr
NM_020975.6:c.2573T>C MANE Select	NP_066124.1:p.Ile858Thr
NM_020630.6:c.2573T>C	NP_065681.1:p.Ile858Thr