Canonical Allele Identifier: CA2608869643

Gene: RET

Linked Data

• gnomAD v4: 10-43106305-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43106305A>G , CM000672.2:g.43106305A>G	GRCh38
NC_000010.10:g.43601753A>G , CM000672.1:g.43601753A>G	GRCh37
NC_000010.9:g.42921759A>G	NCBI36
NG_007489.1:g.34237A>G , LRG_518:g.34237A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.867+1112A>G	ENSP00000480088.2:n.867+1112A>G
ENST00000683007.1:n.442-71A>G
ENST00000340058.6:c.868-71A>G	ENSP00000344798.4:n.868-71A>G
ENST00000355710.8:c.868-71A>G MANE Select	ENSP00000347942.3:n.868-71A>G
ENST00000671844.1:c.625+3676A>G	ENSP00000500541.1:n.625+3676A>G
ENST00000672389.1:c.74-4902A>G	ENSP00000500252.1:n.74-4902A>G
ENST00000340058.5:c.868-71A>G	ENSP00000344798.4:n.868-71A>G
ENST00000355710.7:c.868-71A>G	ENSP00000347942.3:n.868-71A>G
ENST00000479913.1:n.463-71A>G
ENST00000498820.5:c.74-5794A>G	ENSP00000419080.1:n.74-5794A>G
ENST00000615310.4:c.868-71A>G	ENSP00000480088.1:n.868-71A>G
NM_020630.4:c.868-71A>G , LRG_518t2:c.868-71A>G	NP_065681.1:n.868-71A>G
NM_020975.4:c.868-71A>G , LRG_518t1:c.868-71A>G	NP_066124.1:n.868-71A>G
XM_011540027.1:c.868-71A>G	XP_011538329.1:n.868-71A>G
NM_001355216.1:c.106-71A>G	NP_001342145.1:n.106-71A>G
NM_020630.5:c.868-71A>G	NP_065681.1:n.868-71A>G
NM_020975.5:c.868-71A>G	NP_066124.1:n.868-71A>G
NM_020975.6:c.868-71A>G MANE Select	NP_066124.1:n.868-71A>G
NM_020630.6:c.868-71A>G	NP_065681.1:n.868-71A>G