Canonical Allele Identifier: CA9884588

Gene: PCIF1

Linked Data

• dbSNP Id: rs777081786
• ExAC: 20:44575941 G / A
• gnomAD v2: 20-44575941-G-A
• gnomAD v3: 20-45947302-G-A
• gnomAD v4: 20-45947302-G-A
• MyVariant Identifiers: chr20:g.44575941G>A (hg19) ; chr20:g.45947302G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.45947302G>A , CM000682.2:g.45947302G>A	GRCh38
NC_000020.10:g.44575941G>A , CM000682.1:g.44575941G>A	GRCh37
NC_000020.9:g.44009348G>A	NCBI36
NG_029772.1:g.29893C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372409.8:c.1747G>A MANE Select	ENSP00000361486.3:p.Val583Met
ENST00000372409.7:c.1747G>A	ENSP00000361486.3:p.Val583Met
ENST00000479348.2:c.603G>A
NM_022104.3:c.1747G>A	NP_071387.1:p.Val583Met
XM_011528980.1:c.1747G>A	XP_011527282.1:p.Val583Met
XM_011528981.1:c.1747G>A	XP_011527283.1:p.Val583Met
XM_011528982.1:c.703G>A	XP_011527284.1:p.Val235Met
XM_011528980.3:c.1747G>A	XP_011527282.1:p.Val583Met
XM_011528981.3:c.1747G>A	XP_011527283.1:p.Val583Met
XM_017028013.2:c.1747G>A	XP_016883502.1:p.Val583Met
XM_017028014.2:c.703G>A	XP_016883503.1:p.Val235Met
NM_022104.4:c.1747G>A MANE Select	NP_071387.1:p.Val583Met