Canonical Allele Identifier: CA469490418

Gene: RET

Linked Data

• ClinVar Variation Id: 1154058
• ClinVar RCV Id: RCV001495944
• dbSNP Id: rs1800858
• MyVariant Identifiers: chr10:g.43595968A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43100520A>T , CM000672.2:g.43100520A>T	GRCh38
NC_000010.10:g.43595968A>T , CM000672.1:g.43595968A>T	GRCh37
NC_000010.9:g.42915974A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000615310.5:c.135A>T	ENSP00000480088.2:p.Ala45=
ENST00000683278.1:c.37A>T
ENST00000684216.1:c.37A>T
ENST00000340058.6:c.135A>T	ENSP00000344798.4:p.Ala45=
ENST00000355710.8:c.135A>T MANE Select	ENSP00000347942.3:p.Ala45=
ENST00000638465.1:c.37A>T
ENST00000640619.1:c.37A>T
ENST00000671844.1:c.135A>T	ENSP00000500541.1:p.Ala45=
ENST00000672389.1:c.74-10687A>T	ENSP00000500252.1:n.74-10687A>T
ENST00000340058.5:c.135A>T	ENSP00000344798.4:p.Ala45=
ENST00000355710.7:c.135A>T	ENSP00000347942.3:p.Ala45=
ENST00000498820.5:c.74-11579A>T	ENSP00000419080.1:n.74-11579A>T
ENST00000615310.4:c.135A>T	ENSP00000480088.1:p.Ala45=
XM_011540027.1:c.135A>T	XP_011538329.1:p.Ala45=
NM_020630.5:c.135A>T	NP_065681.1:p.Ala45=
NM_020975.5:c.135A>T	NP_066124.1:p.Ala45=
NM_020975.6:c.135A>T MANE Select	NP_066124.1:p.Ala45=
NM_020630.6:c.135A>T	NP_065681.1:p.Ala45=