Canonical Allele Identifier: CA1505986217

Gene: PDGFC

Linked Data

• dbSNP Id: rs1731524185

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.156798990_156798993dup , CM000666.2:g.156798990_156798993dup	GRCh38
NC_000004.11:g.157720142_157720145dup , CM000666.1:g.157720142_157720145dup	GRCh37
NC_000004.10:g.157939592_157939595dup	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000502773.6:c.495+11845_495+11848dup MANE Select	ENSP00000422464.1:n.495+11845_495+11848dup
ENST00000274071.6:c.*403+11845_*403+11848dup	ENSP00000274071.2:n.*403+11845_*403+11848dup
ENST00000422544.2:c.495+11845_495+11848dup	ENSP00000410048.2:n.495+11845_495+11848dup
ENST00000502773.5:c.495+11845_495+11848dup	ENSP00000422464.1:n.495+11845_495+11848dup
ENST00000506880.5:c.149+11845_149+11848dup
ENST00000511985.1:n.55+11845_55+11848dup
ENST00000512711.1:n.418-26099_418-26096dup
NM_016205.2:c.495+11845_495+11848dup	NP_057289.1:n.495+11845_495+11848dup
NR_036641.1:n.1047+11845_1047+11848dup
XM_011532124.1:c.462+11845_462+11848dup	XP_011530426.1:n.462+11845_462+11848dup
XM_011532125.1:c.426+11845_426+11848dup	XP_011530427.1:n.426+11845_426+11848dup
XM_011532124.2:c.462+11845_462+11848dup	XP_011530426.1:n.462+11845_462+11848dup
XM_017008455.1:c.390+11845_390+11848dup	XP_016863944.1:n.390+11845_390+11848dup
XM_017008456.2:c.495+11845_495+11848dup	XP_016863945.1:n.495+11845_495+11848dup
NM_016205.3:c.495+11845_495+11848dup MANE Select	NP_057289.1:n.495+11845_495+11848dup
NR_036641.2:n.1452+11845_1452+11848dup