Canonical Allele Identifier: CA636176181

Gene: PCIF1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.45947864G>A , CM000682.2:g.45947864G>A	GRCh38
NC_000020.10:g.44576503G>A , CM000682.1:g.44576503G>A	GRCh37
NC_000020.9:g.44009910G>A	NCBI36
NG_029772.1:g.29331C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372409.8:c.*109G>A MANE Select	ENSP00000361486.3:n.*109G>A
ENST00000372409.7:c.*109G>A	ENSP00000361486.3:n.*109G>A
ENST00000479348.2:c.1165G>A
NM_022104.3:c.*109G>A	NP_071387.1:n.*109G>A
XM_011528980.1:c.*109G>A	XP_011527282.1:n.*109G>A
XM_011528981.1:c.*109G>A	XP_011527283.1:n.*109G>A
XM_011528982.1:c.*109G>A	XP_011527284.1:n.*109G>A
XM_011528980.3:c.*109G>A	XP_011527282.1:n.*109G>A
XM_011528981.3:c.*109G>A	XP_011527283.1:n.*109G>A
XM_017028013.2:c.*109G>A	XP_016883502.1:n.*109G>A
XM_017028014.2:c.*109G>A	XP_016883503.1:n.*109G>A
NM_022104.4:c.*109G>A MANE Select	NP_071387.1:n.*109G>A