Canonical Allele Identifier: CA1767750407
Gene: PDGFRL HGNC NCBI

Linked Data

dbSNP Id: rs1804221607

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.17604002dup , CM000670.2:g.17604002dup GRCh38
NC_000008.10:g.17461511dup , CM000670.1:g.17461511dup GRCh37
NC_000008.9:g.17505788dup NCBI36
NG_023332.1:g.32570dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000251630.11:c.353+14237dup MANE Select ENSP00000251630.4:n.353+14237dup
ENST00000673645.1:c.353+14237dup ENSP00000501219.1:n.353+14237dup
ENST00000251630.10:c.353+14237dup ENSP00000251630.4:n.353+14237dup
ENST00000541323.1:c.353+14237dup ENSP00000444211.1:n.353+14237dup
NM_006207.2:c.353+14237dup NP_006198.1:n.353+14237dup
XM_011544558.1:c.353+14237dup XP_011542860.1:n.353+14237dup
NM_001372073.1:c.353+14237dup MANE Select NP_001359002.1:n.353+14237dup