Canonical Allele Identifier: CA036415

Gene: RET

Linked Data

• ClinVar Variation Id: 2915939
• ClinVar RCV Id: RCV003647179
• dbSNP Id: rs773428442
• ExAC: 10:43596022 G / A
• gnomAD v2: 10-43596022-G-A
• gnomAD v4: 10-43100574-G-A
• MyVariant Identifiers: chr10:g.43596022G>A (hg19) ; chr10:g.43100574G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43100574G>A , CM000672.2:g.43100574G>A	GRCh38
NC_000010.10:g.43596022G>A , CM000672.1:g.43596022G>A	GRCh37
NC_000010.9:g.42916028G>A	NCBI36
NG_007489.1:g.28506G>A , LRG_518:g.28506G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.189G>A	ENSP00000480088.2:p.Val63=
ENST00000683278.1:c.91G>A
ENST00000684216.1:c.91G>A
ENST00000340058.6:c.189G>A	ENSP00000344798.4:p.Val63=
ENST00000355710.8:c.189G>A MANE Select	ENSP00000347942.3:p.Val63=
ENST00000638465.1:c.91G>A
ENST00000640619.1:c.91G>A
ENST00000671844.1:c.189G>A	ENSP00000500541.1:p.Val63=
ENST00000672389.1:c.74-10633G>A	ENSP00000500252.1:n.74-10633G>A
ENST00000340058.5:c.189G>A	ENSP00000344798.4:p.Val63=
ENST00000355710.7:c.189G>A	ENSP00000347942.3:p.Val63=
ENST00000498820.5:c.74-11525G>A	ENSP00000419080.1:n.74-11525G>A
ENST00000615310.4:c.189G>A	ENSP00000480088.1:p.Val63=
NM_020630.4:c.189G>A , LRG_518t2:c.189G>A	NP_065681.1:p.Val63=
NM_020975.4:c.189G>A , LRG_518t1:c.189G>A	NP_066124.1:p.Val63=
XM_011540027.1:c.189G>A	XP_011538329.1:p.Val63=
NM_020630.5:c.189G>A	NP_065681.1:p.Val63=
NM_020975.5:c.189G>A	NP_066124.1:p.Val63=
NM_020975.6:c.189G>A MANE Select	NP_066124.1:p.Val63=
NM_020630.6:c.189G>A	NP_065681.1:p.Val63=