Canonical Allele Identifier: CA1767750463
Gene: PDGFRL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.17604026_17604027delinsAG , CM000670.2:g.17604026_17604027delinsAG GRCh38
NC_000008.10:g.17461535_17461536delinsAG , CM000670.1:g.17461535_17461536delinsAG GRCh37
NC_000008.9:g.17505812_17505813delinsAG NCBI36
NG_023332.1:g.32594_32595delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000251630.11:c.353+14261_353+14262delinsAG MANE Select ENSP00000251630.4:n.353+14261_353+14262delinsAG
ENST00000673645.1:c.353+14261_353+14262delinsAG ENSP00000501219.1:n.353+14261_353+14262delinsAG
ENST00000251630.10:c.353+14261_353+14262delinsAG ENSP00000251630.4:n.353+14261_353+14262delinsAG
ENST00000541323.1:c.353+14261_353+14262delinsAG ENSP00000444211.1:n.353+14261_353+14262delinsAG
NM_006207.2:c.353+14261_353+14262delinsAG NP_006198.1:n.353+14261_353+14262delinsAG
XM_011544558.1:c.353+14261_353+14262delinsAG XP_011542860.1:n.353+14261_353+14262delinsAG
NM_001372073.1:c.353+14261_353+14262delinsAG MANE Select NP_001359002.1:n.353+14261_353+14262delinsAG