Canonical Allele Identifier: CA2608872443

Gene: RET

Linked Data

• gnomAD v4: 10-43114328-GGT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43114331_43114332del , CM000672.2:g.43114331_43114332del	GRCh38
NC_000010.10:g.43609779_43609780del , CM000672.1:g.43609779_43609780del	GRCh37
NC_000010.9:g.42929785_42929786del	NCBI36
NG_007489.1:g.42263_42264del , LRG_518:g.42263_42264del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.1484-149_1484-148del	ENSP00000480088.2:n.1484-149_1484-148del
ENST00000683007.1:n.1454-149_1454-148del
ENST00000683872.1:n.1296_1297del
ENST00000340058.6:c.1880-149_1880-148del	ENSP00000344798.4:n.1880-149_1880-148del
ENST00000355710.8:c.1880-149_1880-148del MANE Select	ENSP00000347942.3:n.1880-149_1880-148del
ENST00000671844.1:c.*474-149_*474-148del	ENSP00000500541.1:n.*474-149_*474-148del
ENST00000672389.1:c.*474-149_*474-148del	ENSP00000500252.1:n.*474-149_*474-148del
ENST00000340058.5:c.1880-149_1880-148del	ENSP00000344798.4:n.1880-149_1880-148del
ENST00000355710.7:c.1880-149_1880-148del	ENSP00000347942.3:n.1880-149_1880-148del
ENST00000498820.5:c.431-149_431-148del	ENSP00000419080.1:n.431-149_431-148del
ENST00000615310.4:c.1289+3099_1289+3100del	ENSP00000480088.1:n.1289+3099_1289+3100del
NM_020630.4:c.1880-149_1880-148del , LRG_518t2:c.1880-149_1880-148del	NP_065681.1:n.1880-149_1880-148del
NM_020975.4:c.1880-149_1880-148del , LRG_518t1:c.1880-149_1880-148del	NP_066124.1:n.1880-149_1880-148del
XM_011540027.1:c.1880-149_1880-148del	XP_011538329.1:n.1880-149_1880-148del
NM_001355216.1:c.1118-149_1118-148del	NP_001342145.1:n.1118-149_1118-148del
NM_020630.5:c.1880-149_1880-148del	NP_065681.1:n.1880-149_1880-148del
NM_020975.5:c.1880-149_1880-148del	NP_066124.1:n.1880-149_1880-148del
NM_020975.6:c.1880-149_1880-148del MANE Select	NP_066124.1:n.1880-149_1880-148del
NM_020630.6:c.1880-149_1880-148del	NP_065681.1:n.1880-149_1880-148del