Canonical Allele Identifier: CA2588645648

Gene: RET

Linked Data

• gnomAD v3: 10-43100761-CCACCCCTTCCTCAAGCCGCCCTTATCACAGCCGCTGACACTGAAGCTTGGCATGGCTT-C
• gnomAD v4: 10-43100761-CCACCCCTTCCTCAAGCCGCCCTTATCACAGCCGCTGACACTGAAGCTTGGCATGGCTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43100763_43100820del , CM000672.2:g.43100763_43100820del	GRCh38
NC_000010.10:g.43596211_43596268del , CM000672.1:g.43596211_43596268del	GRCh37
NC_000010.9:g.42916217_42916274del	NCBI36
NG_007489.1:g.28695_28752del , LRG_518:g.28695_28752del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.337+41_337+98del	ENSP00000480088.2:n.337+41_337+98del
ENST00000683278.1:c.239+41_239+98del
ENST00000684216.1:c.239+41_239+98del
ENST00000340058.6:c.337+41_337+98del	ENSP00000344798.4:n.337+41_337+98del
ENST00000355710.8:c.337+41_337+98del MANE Select	ENSP00000347942.3:n.337+41_337+98del
ENST00000638465.1:c.239+41_239+98del
ENST00000640619.1:c.239+41_239+98del
ENST00000671844.1:c.337+41_337+98del	ENSP00000500541.1:n.337+41_337+98del
ENST00000672389.1:c.74-10444_74-10387del	ENSP00000500252.1:n.74-10444_74-10387del
ENST00000340058.5:c.337+41_337+98del	ENSP00000344798.4:n.337+41_337+98del
ENST00000355710.7:c.337+41_337+98del	ENSP00000347942.3:n.337+41_337+98del
ENST00000498820.5:c.74-11336_74-11279del	ENSP00000419080.1:n.74-11336_74-11279del
ENST00000615310.4:c.337+41_337+98del	ENSP00000480088.1:n.337+41_337+98del
NM_020630.4:c.337+41_337+98del , LRG_518t2:c.337+41_337+98del	NP_065681.1:n.337+41_337+98del
NM_020975.4:c.337+41_337+98del , LRG_518t1:c.337+41_337+98del	NP_066124.1:n.337+41_337+98del
XM_011540027.1:c.337+41_337+98del	XP_011538329.1:n.337+41_337+98del
NM_020630.5:c.337+41_337+98del	NP_065681.1:n.337+41_337+98del
NM_020975.5:c.337+41_337+98del	NP_066124.1:n.337+41_337+98del
NM_020975.6:c.337+41_337+98del MANE Select	NP_066124.1:n.337+41_337+98del
NM_020630.6:c.337+41_337+98del	NP_065681.1:n.337+41_337+98del