Canonical Allele Identifier: CA2653107639

Gene: PCIF1

Linked Data

• gnomAD v4: 20-45947769-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.45947769G>T , CM000682.2:g.45947769G>T	GRCh38
NC_000020.10:g.44576408G>T , CM000682.1:g.44576408G>T	GRCh37
NC_000020.9:g.44009815G>T	NCBI36
NG_029772.1:g.29426C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000372409.8:c.*14G>T MANE Select	ENSP00000361486.3:n.*14G>T
ENST00000372409.7:c.*14G>T	ENSP00000361486.3:n.*14G>T
ENST00000479348.2:c.1070G>T
NM_022104.3:c.*14G>T	NP_071387.1:n.*14G>T
XM_011528980.1:c.*14G>T	XP_011527282.1:n.*14G>T
XM_011528981.1:c.*14G>T	XP_011527283.1:n.*14G>T
XM_011528982.1:c.*14G>T	XP_011527284.1:n.*14G>T
XM_011528980.3:c.*14G>T	XP_011527282.1:n.*14G>T
XM_011528981.3:c.*14G>T	XP_011527283.1:n.*14G>T
XM_017028013.2:c.*14G>T	XP_016883502.1:n.*14G>T
XM_017028014.2:c.*14G>T	XP_016883503.1:n.*14G>T
NM_022104.4:c.*14G>T MANE Select	NP_071387.1:n.*14G>T