Canonical Allele Identifier: CA1767749931
Gene: PDGFRL HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.17603706T= , CM000670.2:g.17603706T= GRCh38
NC_000008.10:g.17461215T= , CM000670.1:g.17461215T= GRCh37
NC_000008.9:g.17505492T= NCBI36
NG_023332.1:g.32274T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000251630.11:c.353+13941T= MANE Select ENSP00000251630.4:n.353+13941T=
ENST00000673645.1:c.353+13941T= ENSP00000501219.1:n.353+13941T=
ENST00000251630.10:c.353+13941T= ENSP00000251630.4:n.353+13941T=
ENST00000541323.1:c.353+13941T= ENSP00000444211.1:n.353+13941T=
NM_006207.2:c.353+13941T= NP_006198.1:n.353+13941T=
XM_011544558.1:c.353+13941T= XP_011542860.1:n.353+13941T=
NM_001372073.1:c.353+13941T= MANE Select NP_001359002.1:n.353+13941T=
Search 100 bp 5'
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