Canonical Allele Identifier: CA2608875616

Gene: RET

Linked Data

• gnomAD v4: 10-43119805-CGCCCCTGCCACCCACACCCTGGCCTGCCACTCCCCCACCATGCCACACTCTAGCCCACCAT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43119816_43119876del , CM000672.2:g.43119816_43119876del	GRCh38
NC_000010.10:g.43615264_43615324del , CM000672.1:g.43615264_43615324del	GRCh37
NC_000010.9:g.42935270_42935330del	NCBI36
NG_007489.1:g.47748_47808del , LRG_518:g.47748_47808del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.2211+71_2211+131del	ENSP00000480088.2:n.2211+71_2211+131del
ENST00000683007.1:n.2181+71_2181+131del
ENST00000683872.1:n.2172+71_2172+131del
ENST00000340058.6:c.2607+71_2607+131del	ENSP00000344798.4:n.2607+71_2607+131del
ENST00000355710.8:c.2607+71_2607+131del MANE Select	ENSP00000347942.3:n.2607+71_2607+131del
ENST00000671844.1:c.*1201+71_*1201+131del	ENSP00000500541.1:n.*1201+71_*1201+131del
ENST00000672389.1:c.*1201+71_*1201+131del	ENSP00000500252.1:n.*1201+71_*1201+131del
ENST00000340058.5:c.2607+71_2607+131del	ENSP00000344798.4:n.2607+71_2607+131del
ENST00000355710.7:c.2607+71_2607+131del	ENSP00000347942.3:n.2607+71_2607+131del
ENST00000615310.4:c.1333+71_1333+131del	ENSP00000480088.1:n.1333+71_1333+131del
NM_020630.4:c.2607+71_2607+131del , LRG_518t2:c.2607+71_2607+131del	NP_065681.1:n.2607+71_2607+131del
NM_020975.4:c.2607+71_2607+131del , LRG_518t1:c.2607+71_2607+131del	NP_066124.1:n.2607+71_2607+131del
XM_011540027.1:c.2607+71_2607+131del	XP_011538329.1:n.2607+71_2607+131del
NM_001355216.1:c.1845+71_1845+131del	NP_001342145.1:n.1845+71_1845+131del
NM_020630.5:c.2607+71_2607+131del	NP_065681.1:n.2607+71_2607+131del
NM_020975.5:c.2607+71_2607+131del	NP_066124.1:n.2607+71_2607+131del
NM_020975.6:c.2607+71_2607+131del MANE Select	NP_066124.1:n.2607+71_2607+131del
NM_020630.6:c.2607+71_2607+131del	NP_065681.1:n.2607+71_2607+131del