Canonical Allele Identifier: CA1767750012
Gene: PDGFRL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.17603752_17603756delinsCAATT , CM000670.2:g.17603752_17603756delinsCAATT GRCh38
NC_000008.10:g.17461261_17461265delinsCAATT , CM000670.1:g.17461261_17461265delinsCAATT GRCh37
NC_000008.9:g.17505538_17505542delinsCAATT NCBI36
NG_023332.1:g.32320_32324delinsCAATT

Transcript Alleles

HGVS Amino-acid Change
ENST00000251630.11:c.353+13987_353+13991delinsCAATT MANE Select ENSP00000251630.4:n.353+13987_353+13991delinsCAATT
ENST00000673645.1:c.353+13987_353+13991delinsCAATT ENSP00000501219.1:n.353+13987_353+13991delinsCAATT
ENST00000251630.10:c.353+13987_353+13991delinsCAATT ENSP00000251630.4:n.353+13987_353+13991delinsCAATT
ENST00000541323.1:c.353+13987_353+13991delinsCAATT ENSP00000444211.1:n.353+13987_353+13991delinsCAATT
NM_006207.2:c.353+13987_353+13991delinsCAATT NP_006198.1:n.353+13987_353+13991delinsCAATT
XM_011544558.1:c.353+13987_353+13991delinsCAATT XP_011542860.1:n.353+13987_353+13991delinsCAATT
NM_001372073.1:c.353+13987_353+13991delinsCAATT MANE Select NP_001359002.1:n.353+13987_353+13991delinsCAATT