Canonical Allele Identifier: CA376543214

Gene: RET

Linked Data

• ClinVar Variation Id: 568416
• ClinVar RCV Id: RCV000688770 ; RCV001103793 ; RCV001103794 ; RCV001103791 ; RCV001103792
• dbSNP Id: rs1564490122
• MyVariant Identifiers: chr10:g.43597936C>T (hg19) ; chr10:g.43102488C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43102488C>T , CM000672.2:g.43102488C>T	GRCh38
NC_000010.10:g.43597936C>T , CM000672.1:g.43597936C>T	GRCh37
NC_000010.9:g.42917942C>T	NCBI36
NG_007489.1:g.30420C>T , LRG_518:g.30420C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.484C>T	ENSP00000480088.2:p.Pro162Ser
ENST00000683278.1:c.405C>T
ENST00000684216.1:c.386C>T
ENST00000340058.6:c.484C>T	ENSP00000344798.4:p.Pro162Ser
ENST00000355710.8:c.484C>T MANE Select	ENSP00000347942.3:p.Pro162Ser
ENST00000638465.1:c.426C>T
ENST00000640619.1:c.257C>T
ENST00000671844.1:c.484C>T	ENSP00000500541.1:p.Pro162Ser
ENST00000672389.1:c.74-8719C>T	ENSP00000500252.1:n.74-8719C>T
ENST00000340058.5:c.484C>T	ENSP00000344798.4:p.Pro162Ser
ENST00000355710.7:c.484C>T	ENSP00000347942.3:p.Pro162Ser
ENST00000498820.5:c.74-9611C>T	ENSP00000419080.1:n.74-9611C>T
ENST00000615310.4:c.484C>T	ENSP00000480088.1:p.Pro162Ser
NM_020630.4:c.484C>T , LRG_518t2:c.484C>T	NP_065681.1:p.Pro162Ser
NM_020975.4:c.484C>T , LRG_518t1:c.484C>T	NP_066124.1:p.Pro162Ser
XM_011540027.1:c.484C>T	XP_011538329.1:p.Pro162Ser
NM_020630.5:c.484C>T	NP_065681.1:p.Pro162Ser
NM_020975.5:c.484C>T	NP_066124.1:p.Pro162Ser
NM_020975.6:c.484C>T MANE Select	NP_066124.1:p.Pro162Ser
NM_020630.6:c.484C>T	NP_065681.1:p.Pro162Ser