Canonical Allele Identifier: CA1767749947
Gene: PDGFRL HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.17603718C= , CM000670.2:g.17603718C= GRCh38
NC_000008.10:g.17461227C= , CM000670.1:g.17461227C= GRCh37
NC_000008.9:g.17505504C= NCBI36
NG_023332.1:g.32286C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000251630.11:c.353+13953C= MANE Select ENSP00000251630.4:n.353+13953C=
ENST00000673645.1:c.353+13953C= ENSP00000501219.1:n.353+13953C=
ENST00000251630.10:c.353+13953C= ENSP00000251630.4:n.353+13953C=
ENST00000541323.1:c.353+13953C= ENSP00000444211.1:n.353+13953C=
NM_006207.2:c.353+13953C= NP_006198.1:n.353+13953C=
XM_011544558.1:c.353+13953C= XP_011542860.1:n.353+13953C=
NM_001372073.1:c.353+13953C= MANE Select NP_001359002.1:n.353+13953C=
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