Canonical Allele Identifier: CA927678530

Gene: RET

Linked Data

• gnomAD v3: 10-43119934-C-CGCCCCTGCCATGCCACACCCTGACTCCACCAT
• gnomAD v4: 10-43119934-C-CGCCCCTGCCATGCCACACCCTGACTCCACCAT

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43119954_43119955insTGACTCCACCATGCCCCTGCCATGCCACACCC , CM000672.2:g.43119954_43119955insTGACTCCACCATGCCCCTGCCATGCCACACCC	GRCh38
NC_000010.10:g.43615402_43615403insTGACTCCACCATGCCCCTGCCATGCCACACCC , CM000672.1:g.43615402_43615403insTGACTCCACCATGCCCCTGCCATGCCACACCC	GRCh37
NC_000010.9:g.42935408_42935409insTGACTCCACCATGCCCCTGCCATGCCACACCC	NCBI36
NG_007489.1:g.47886_47887insTGACTCCACCATGCCCCTGCCATGCCACACCC , LRG_518:g.47886_47887insTGACTCCACCATGCCCCTGCCATGCCACACCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.2212-127_2212-126insTGACTCCACCATGCCCCTGCCATGCCACACCC	ENSP00000480088.2:n.2212-127_2212-126insTGACTCCACCATGCCCCTGCC...
ENST00000683007.1:n.2182-127_2182-126insTGACTCCACCATGCCCCTGCCATGCCACACCC
ENST00000683872.1:n.2173-127_2173-126insTGACTCCACCATGCCCCTGCCATGCCACACCC
ENST00000340058.6:c.2608-127_2608-126insTGACTCCACCATGCCCCTGCCATGCCACACCC	ENSP00000344798.4:n.2608-127_2608-126insTGACTCCACCATGCCCCTGCC...
ENST00000355710.8:c.2608-127_2608-126insTGACTCCACCATGCCCCTGCCATGCCACACCC MANE Select	ENSP00000347942.3:n.2608-127_2608-126insTGACTCCACCATGCCCCTGCC...
ENST00000671844.1:c.*1202-127_*1202-126insTGACTCCACCATGCCCCTGCCATGCCACACCC	ENSP00000500541.1:n.*1202-127_*1202-126insTGACTCCACCATGCCCCTG...
ENST00000672389.1:c.*1202-127_*1202-126insTGACTCCACCATGCCCCTGCCATGCCACACCC	ENSP00000500252.1:n.*1202-127_*1202-126insTGACTCCACCATGCCCCTG...
ENST00000340058.5:c.2608-127_2608-126insTGACTCCACCATGCCCCTGCCATGCCACACCC	ENSP00000344798.4:n.2608-127_2608-126insTGACTCCACCATGCCCCTGCC...
ENST00000355710.7:c.2608-127_2608-126insTGACTCCACCATGCCCCTGCCATGCCACACCC	ENSP00000347942.3:n.2608-127_2608-126insTGACTCCACCATGCCCCTGCC...
ENST00000615310.4:c.1334-127_1334-126insTGACTCCACCATGCCCCTGCCATGCCACACCC	ENSP00000480088.1:n.1334-127_1334-126insTGACTCCACCATGCCCCTGCC...
NM_020630.4:c.2608-127_2608-126insTGACTCCACCATGCCCCTGCCATGCCACACCC , LRG_518t2:c.2608-127_2608-126insTGACTCCACCATGCCCCTGCCATGCCACACCC	NP_065681.1:n.2608-127_2608-126insTGACTCCACCATGCCCCTGCCATGCCA...
NM_020975.4:c.2608-127_2608-126insTGACTCCACCATGCCCCTGCCATGCCACACCC , LRG_518t1:c.2608-127_2608-126insTGACTCCACCATGCCCCTGCCATGCCACACCC	NP_066124.1:n.2608-127_2608-126insTGACTCCACCATGCCCCTGCCATGCCA...
XM_011540027.1:c.2608-127_2608-126insTGACTCCACCATGCCCCTGCCATGCCACACCC	XP_011538329.1:n.2608-127_2608-126insTGACTCCACCATGCCCCTGCCATG...
NM_001355216.1:c.1846-127_1846-126insTGACTCCACCATGCCCCTGCCATGCCACACCC	NP_001342145.1:n.1846-127_1846-126insTGACTCCACCATGCCCCTGCCATG...
NM_020630.5:c.2608-127_2608-126insTGACTCCACCATGCCCCTGCCATGCCACACCC	NP_065681.1:n.2608-127_2608-126insTGACTCCACCATGCCCCTGCCATGCCA...
NM_020975.5:c.2608-127_2608-126insTGACTCCACCATGCCCCTGCCATGCCACACCC	NP_066124.1:n.2608-127_2608-126insTGACTCCACCATGCCCCTGCCATGCCA...
NM_020975.6:c.2608-127_2608-126insTGACTCCACCATGCCCCTGCCATGCCACACCC MANE Select	NP_066124.1:n.2608-127_2608-126insTGACTCCACCATGCCCCTGCCATGCCA...
NM_020630.6:c.2608-127_2608-126insTGACTCCACCATGCCCCTGCCATGCCACACCC	NP_065681.1:n.2608-127_2608-126insTGACTCCACCATGCCCCTGCCATGCCA...