Canonical Allele Identifier: CA369945734

Gene: TDRP

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.494582A>C , CM000670.2:g.494582A>C	GRCh38
NC_000008.10:g.444582A>C , CM000670.1:g.444582A>C	GRCh37
NC_000008.9:g.434582A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001384899.1:c.124T>G MANE Select	NP_001371828.1:p.Phe42Val
ENST00000324079.11:c.124T>G MANE Select	ENSP00000315111.6:p.Phe42Val
NM_001256113.1:c.124T>G	NP_001243042.1:p.Phe42Val
NM_001256113.2:c.124T>G	NP_001243042.1:p.Phe42Val
NM_001369716.1:c.154T>G	NP_001356645.1:p.Phe52Val
NM_175075.4:c.124T>G	NP_778250.2:p.Phe42Val
NM_175075.5:c.124T>G	NP_778250.2:p.Phe42Val
ENST00000324079.10:c.124T>G	ENSP00000315111.6:p.Phe42Val
ENST00000427263.6:c.124T>G	ENSP00000408126.2:p.Phe42Val
ENST00000523656.5:c.124T>G	ENSP00000430325.1:p.Phe42Val
ENST00000524229.1:n.55T>G
ENST00000613071.1:c.124T>G	ENSP00000479558.1:p.Phe42Val
XM_006716232.2:c.124T>G	XP_006716295.1:p.Phe42Val
XM_006716232.4:c.124T>G	XP_006716295.1:p.Phe42Val
XM_011534717.1:c.226T>G	XP_011533019.1:p.Phe76Val
XM_011534718.1:c.160T>G	XP_011533020.1:p.Phe54Val
XM_011534719.1:c.154T>G	XP_011533021.1:p.Phe52Val
XM_011534720.1:c.124T>G	XP_011533022.1:p.Phe42Val
XM_011534721.1:c.19T>G	XP_011533023.1:p.Phe7Val
XM_011534722.1:c.226T>G	XP_011533024.1:p.Phe76Val
XM_011534724.1:c.247T>G	XP_011533026.1:p.Phe83Val
XM_011534725.1:c.247T>G	XP_011533027.1:p.Phe83Val
XM_017013113.2:c.154T>G	XP_016868602.1:p.Phe52Val
XR_941338.1:n.241T>G