Canonical Allele Identifier: CA045387

Gene: RET

Linked Data

• dbSNP Id: rs779849973
• ExAC: 10:43601844 G / C
• gnomAD v2: 10-43601844-G-C
• gnomAD v4: 10-43106396-G-C
• MyVariant Identifiers: chr10:g.43601844G>C (hg19) ; chr10:g.43106396G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43106396G>C , CM000672.2:g.43106396G>C	GRCh38
NC_000010.10:g.43601844G>C , CM000672.1:g.43601844G>C	GRCh37
NC_000010.9:g.42921850G>C	NCBI36
NG_007489.1:g.34328G>C , LRG_518:g.34328G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000615310.5:c.867+1203G>C	ENSP00000480088.2:n.867+1203G>C
ENST00000683007.1:n.462G>C
ENST00000340058.6:c.888G>C	ENSP00000344798.4:p.Leu296=
ENST00000355710.8:c.888G>C MANE Select	ENSP00000347942.3:p.Leu296=
ENST00000671844.1:c.625+3767G>C	ENSP00000500541.1:n.625+3767G>C
ENST00000672389.1:c.74-4811G>C	ENSP00000500252.1:n.74-4811G>C
ENST00000340058.5:c.888G>C	ENSP00000344798.4:p.Leu296=
ENST00000355710.7:c.888G>C	ENSP00000347942.3:p.Leu296=
ENST00000479913.1:n.483G>C
ENST00000498820.5:c.74-5703G>C	ENSP00000419080.1:n.74-5703G>C
ENST00000615310.4:c.888G>C	ENSP00000480088.1:p.Leu296=
NM_020630.4:c.888G>C , LRG_518t2:c.888G>C	NP_065681.1:p.Leu296=
NM_020975.4:c.888G>C , LRG_518t1:c.888G>C	NP_066124.1:p.Leu296=
XM_011540027.1:c.888G>C	XP_011538329.1:p.Leu296=
NM_001355216.1:c.126G>C	NP_001342145.1:p.Leu42=
NM_020630.5:c.888G>C	NP_065681.1:p.Leu296=
NM_020975.5:c.888G>C	NP_066124.1:p.Leu296=
NM_020975.6:c.888G>C MANE Select	NP_066124.1:p.Leu296=
NM_020630.6:c.888G>C	NP_065681.1:p.Leu296=