Canonical Allele Identifier: CA357398176

Gene: PRDM8

Linked Data

• gnomAD v4: 4-80202553-T-C
• MyVariant Identifiers: chr4:g.81123707T>C (hg19) ; chr4:g.80202553T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.80202553T>C , CM000666.2:g.80202553T>C	GRCh38
NC_000004.11:g.81123707T>C , CM000666.1:g.81123707T>C	GRCh37
NC_000004.10:g.81342731T>C	NCBI36
NG_046725.1:g.22284T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415738.3:c.1091T>C MANE Select	ENSP00000406998.2:p.Leu364Pro
ENST00000339711.8:c.1091T>C	ENSP00000339764.4:p.Leu364Pro
ENST00000415738.2:c.1091T>C	ENSP00000406998.2:p.Leu364Pro
ENST00000504452.5:c.1091T>C	ENSP00000423985.1:p.Leu364Pro
ENST00000515013.5:c.1091T>C	ENSP00000425149.1:p.Leu364Pro
NM_001099403.1:c.1091T>C	NP_001092873.1:p.Leu364Pro
NM_020226.3:c.1091T>C	NP_064611.3:p.Leu364Pro
XM_005263144.2:c.1094T>C	XP_005263201.1:p.Leu365Pro
XM_005263145.2:c.1094T>C	XP_005263202.1:p.Leu365Pro
XM_005263146.3:c.1091T>C	XP_005263203.1:p.Leu364Pro
XM_011532133.1:c.1934T>C	XP_011530435.1:p.Leu645Pro
XM_011532134.1:c.1931T>C	XP_011530436.1:p.Leu644Pro
XM_011532135.1:c.1793T>C	XP_011530437.1:p.Leu598Pro
XM_011532136.1:c.1646T>C	XP_011530438.1:p.Leu549Pro
XM_011532137.1:c.1646T>C	XP_011530439.1:p.Leu549Pro
XM_011532138.1:c.1646T>C	XP_011530440.1:p.Leu549Pro
XM_011532139.1:c.1646T>C	XP_011530441.1:p.Leu549Pro
XM_011532140.1:c.1646T>C	XP_011530442.1:p.Leu549Pro
XM_011532141.1:c.1508T>C	XP_011530443.1:p.Leu503Pro
XM_011532142.1:c.1487T>C	XP_011530444.1:p.Leu496Pro
XM_005263146.4:c.1091T>C	XP_005263203.1:p.Leu364Pro
XM_011532133.2:c.1934T>C	XP_011530435.1:p.Leu645Pro
XM_011532135.2:c.1793T>C	XP_011530437.1:p.Leu598Pro
XM_011532140.2:c.1646T>C	XP_011530442.1:p.Leu549Pro
XM_011532141.3:c.1508T>C	XP_011530443.1:p.Leu503Pro
XM_017008468.1:c.1643T>C	XP_016863957.1:p.Leu548Pro
XM_017008469.1:c.1730T>C	XP_016863958.1:p.Leu577Pro
XM_017008470.1:c.1646T>C	XP_016863959.1:p.Leu549Pro
NM_001099403.2:c.1091T>C MANE Select	NP_001092873.1:p.Leu364Pro
NM_020226.4:c.1091T>C	NP_064611.3:p.Leu364Pro