Canonical Allele Identifier: CA592895804

Gene: RET

Linked Data

• dbSNP Id: rs1189091304
• gnomAD v2: 10-43613757-G-C
• gnomAD v3: 10-43118309-G-C
• gnomAD v4: 10-43118309-G-C
• MyVariant Identifiers: chr10:g.43613757G>C (hg19) ; chr10:g.43118309G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43118309G>C , CM000672.2:g.43118309G>C	GRCh38
NC_000010.10:g.43613757G>C , CM000672.1:g.43613757G>C	GRCh37
NC_000010.9:g.42933763G>C	NCBI36
NG_007489.1:g.46241G>C , LRG_518:g.46241G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000615310.5:c.1889-64G>C	ENSP00000480088.2:n.1889-64G>C
ENST00000683007.1:n.1859-64G>C
ENST00000683872.1:n.1850-64G>C
ENST00000340058.6:c.2285-64G>C	ENSP00000344798.4:n.2285-64G>C
ENST00000355710.8:c.2285-64G>C MANE Select	ENSP00000347942.3:n.2285-64G>C
ENST00000671844.1:c.*879-64G>C	ENSP00000500541.1:n.*879-64G>C
ENST00000672389.1:c.*879-64G>C	ENSP00000500252.1:n.*879-64G>C
ENST00000340058.5:c.2285-64G>C	ENSP00000344798.4:n.2285-64G>C
ENST00000355710.7:c.2285-64G>C	ENSP00000347942.3:n.2285-64G>C
ENST00000615310.4:c.1290-1393G>C	ENSP00000480088.1:n.1290-1393G>C
NM_020630.4:c.2285-64G>C , LRG_518t2:c.2285-64G>C	NP_065681.1:n.2285-64G>C
NM_020975.4:c.2285-64G>C , LRG_518t1:c.2285-64G>C	NP_066124.1:n.2285-64G>C
XM_011540027.1:c.2285-64G>C	XP_011538329.1:n.2285-64G>C
NM_001355216.1:c.1523-64G>C	NP_001342145.1:n.1523-64G>C
NM_020630.5:c.2285-64G>C	NP_065681.1:n.2285-64G>C
NM_020975.5:c.2285-64G>C	NP_066124.1:n.2285-64G>C
NM_020975.6:c.2285-64G>C MANE Select	NP_066124.1:n.2285-64G>C
NM_020630.6:c.2285-64G>C	NP_065681.1:n.2285-64G>C