Canonical Allele Identifier: CA9428083

Gene: PAF1 SAMD4B

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39388317C>G , CM000681.2:g.39388317C>G	GRCh38
NC_000019.9:g.39878957C>G , CM000681.1:g.39878957C>G	GRCh37
NC_000019.8:g.44570797C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_019088.4:c.986+22G>C (PAF1) MANE Select	NP_061961.2:n.986+22G>C
ENST00000221265.8:c.986+22G>C (PAF1) MANE Select	ENSP00000221265.2:n.986+22G>C
NM_001256826.1:c.956+22G>C (PAF1)	NP_001243755.1:n.956+22G>C
NM_001256826.2:c.956+22G>C (PAF1)	NP_001243755.1:n.956+22G>C
NM_019088.3:c.986+22G>C (PAF1)	NP_061961.2:n.986+22G>C
NR_046384.1:n.1195+22G>C (PAF1)
NR_046384.2:n.1106+22G>C (PAF1)
ENST00000221265.7:c.986+22G>C (PAF1)	ENSP00000221265.2:n.986+22G>C
ENST00000416728.3:c.827+22G>C (PAF1)	ENSP00000396412.2:n.827+22G>C
ENST00000595564.5:c.956+22G>C (PAF1)	ENSP00000468874.1:n.956+22G>C
XM_011527057.1:c.2057-2209C>G (SAMD4B)	XP_011525359.1:n.2057-2209C>G
XM_011527057.2:c.2057-2209C>G (SAMD4B)	XP_011525359.1:n.2057-2209C>G
XM_011527058.1:c.2057-2209C>G (SAMD4B)	XP_011525360.1:n.2057-2209C>G
XM_011527059.1:c.2057-2209C>G (SAMD4B)	XP_011525361.1:n.2057-2209C>G
XM_011527060.1:c.2057-2209C>G (SAMD4B)	XP_011525362.1:n.2057-2209C>G
XM_011527060.3:c.2057-2209C>G (SAMD4B)	XP_011525362.1:n.2057-2209C>G
XM_011527061.1:c.2057-2209C>G (SAMD4B)	XP_011525363.1:n.2057-2209C>G
XM_011527061.3:c.2057-2209C>G (SAMD4B)	XP_011525363.1:n.2057-2209C>G
XM_011527062.1:c.2057-2209C>G (SAMD4B)	XP_011525364.1:n.2057-2209C>G
XM_011527062.2:c.2057-2209C>G (SAMD4B)	XP_011525364.1:n.2057-2209C>G
XM_017026918.1:c.2057-2209C>G (SAMD4B)	XP_016882407.1:n.2057-2209C>G
XM_017026919.1:c.2057-2209C>G (SAMD4B)	XP_016882408.1:n.2057-2209C>G