Canonical Allele Identifier: CA592895831

Gene: RET

Linked Data

• dbSNP Id: rs1267801014
• gnomAD v2: 10-43613953-G-T
• gnomAD v4: 10-43118505-G-T
• MyVariant Identifiers: chr10:g.43613953G>T (hg19) ; chr10:g.43118505G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43118505G>T , CM000672.2:g.43118505G>T	GRCh38
NC_000010.10:g.43613953G>T , CM000672.1:g.43613953G>T	GRCh37
NC_000010.9:g.42933959G>T	NCBI36
NG_007489.1:g.46437G>T , LRG_518:g.46437G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.1996+25G>T	ENSP00000480088.2:n.1996+25G>T
ENST00000683007.1:n.1966+25G>T
ENST00000683872.1:n.1957+25G>T
ENST00000340058.6:c.2392+25G>T	ENSP00000344798.4:n.2392+25G>T
ENST00000355710.8:c.2392+25G>T MANE Select	ENSP00000347942.3:n.2392+25G>T
ENST00000671844.1:c.*986+25G>T	ENSP00000500541.1:n.*986+25G>T
ENST00000672389.1:c.*986+25G>T	ENSP00000500252.1:n.*986+25G>T
ENST00000340058.5:c.2392+25G>T	ENSP00000344798.4:n.2392+25G>T
ENST00000355710.7:c.2392+25G>T	ENSP00000347942.3:n.2392+25G>T
ENST00000615310.4:c.1290-1197G>T	ENSP00000480088.1:n.1290-1197G>T
NM_020630.4:c.2392+25G>T , LRG_518t2:c.2392+25G>T	NP_065681.1:n.2392+25G>T
NM_020975.4:c.2392+25G>T , LRG_518t1:c.2392+25G>T	NP_066124.1:n.2392+25G>T
XM_011540027.1:c.2392+25G>T	XP_011538329.1:n.2392+25G>T
NM_001355216.1:c.1630+25G>T	NP_001342145.1:n.1630+25G>T
NM_020630.5:c.2392+25G>T	NP_065681.1:n.2392+25G>T
NM_020975.5:c.2392+25G>T	NP_066124.1:n.2392+25G>T
NM_020975.6:c.2392+25G>T MANE Select	NP_066124.1:n.2392+25G>T
NM_020630.6:c.2392+25G>T	NP_065681.1:n.2392+25G>T