Canonical Allele Identifier: CA13219590

Gene: RET

Linked Data

• ClinVar Variation Id: 1222122
• ClinVar RCV Id: RCV001595940
• dbSNP Id: rs2742243
• gnomAD v2: 10-43601749-T-C
• gnomAD v3: 10-43106301-T-C
• gnomAD v4: 10-43106301-T-C
• MyVariant Identifiers: chr10:g.43601749T>C (hg19) ; chr10:g.43106301T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43106301T>C , CM000672.2:g.43106301T>C	GRCh38
NC_000010.10:g.43601749T>C , CM000672.1:g.43601749T>C	GRCh37
NC_000010.9:g.42921755T>C	NCBI36
NG_007489.1:g.34233T>C , LRG_518:g.34233T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.867+1108T>C	ENSP00000480088.2:n.867+1108T>C
ENST00000683007.1:n.442-75T>C
ENST00000340058.6:c.868-75T>C	ENSP00000344798.4:n.868-75T>C
ENST00000355710.8:c.868-75T>C MANE Select	ENSP00000347942.3:n.868-75T>C
ENST00000671844.1:c.625+3672T>C	ENSP00000500541.1:n.625+3672T>C
ENST00000672389.1:c.74-4906T>C	ENSP00000500252.1:n.74-4906T>C
ENST00000340058.5:c.868-75T>C	ENSP00000344798.4:n.868-75T>C
ENST00000355710.7:c.868-75T>C	ENSP00000347942.3:n.868-75T>C
ENST00000479913.1:n.463-75T>C
ENST00000498820.5:c.74-5798T>C	ENSP00000419080.1:n.74-5798T>C
ENST00000615310.4:c.868-75T>C	ENSP00000480088.1:n.868-75T>C
NM_020630.4:c.868-75T>C , LRG_518t2:c.868-75T>C	NP_065681.1:n.868-75T>C
NM_020975.4:c.868-75T>C , LRG_518t1:c.868-75T>C	NP_066124.1:n.868-75T>C
XM_011540027.1:c.868-75T>C	XP_011538329.1:n.868-75T>C
NM_001355216.1:c.106-75T>C	NP_001342145.1:n.106-75T>C
NM_020630.5:c.868-75T>C	NP_065681.1:n.868-75T>C
NM_020975.5:c.868-75T>C	NP_066124.1:n.868-75T>C
NM_020975.6:c.868-75T>C MANE Select	NP_066124.1:n.868-75T>C
NM_020630.6:c.868-75T>C	NP_065681.1:n.868-75T>C