Canonical Allele Identifier: CA469279451

Gene: RET

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43102448C>T , CM000672.2:g.43102448C>T	GRCh38
NC_000010.10:g.43597896C>T , CM000672.1:g.43597896C>T	GRCh37
NC_000010.9:g.42917902C>T	NCBI36
NG_007489.1:g.30380C>T , LRG_518:g.30380C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_020975.6:c.444C>T MANE Select	NP_066124.1:p.Ser148=
ENST00000355710.8:c.444C>T MANE Select	ENSP00000347942.3:p.Ser148=
NM_020630.4:c.444C>T , LRG_518t2:c.444C>T	NP_065681.1:p.Ser148=
NM_020630.5:c.444C>T	NP_065681.1:p.Ser148=
NM_020630.6:c.444C>T	NP_065681.1:p.Ser148=
NM_020975.4:c.444C>T , LRG_518t1:c.444C>T	NP_066124.1:p.Ser148=
NM_020975.5:c.444C>T	NP_066124.1:p.Ser148=
ENST00000340058.5:c.444C>T	ENSP00000344798.4:p.Ser148=
ENST00000340058.6:c.444C>T	ENSP00000344798.4:p.Ser148=
ENST00000355710.7:c.444C>T	ENSP00000347942.3:p.Ser148=
ENST00000498820.5:c.74-9651C>T	ENSP00000419080.1:n.74-9651C>T
ENST00000615310.4:c.444C>T	ENSP00000480088.1:p.Ser148=
ENST00000615310.5:c.444C>T	ENSP00000480088.2:p.Ser148=
ENST00000638465.1:c.386C>T
ENST00000640619.1:c.240-23C>T
ENST00000671844.1:c.444C>T	ENSP00000500541.1:p.Ser148=
ENST00000672389.1:c.74-8759C>T	ENSP00000500252.1:n.74-8759C>T
ENST00000683278.1:c.365C>T
ENST00000684216.1:c.346C>T
XM_011540027.1:c.444C>T	XP_011538329.1:p.Ser148=