Canonical Allele Identifier: CA553082750

Gene: PRDM8

Linked Data

• dbSNP Id: rs1560477758
• gnomAD v2: 4-81123588-C-CGGTGGCGCT
• gnomAD v4: 4-80202434-C-CGGTGGCGCT
• MyVariant Identifiers: chr4:g.81123588_81123589insGGTGGCGCT (hg19) ; chr4:g.80202434_80202435insGGTGGCGCT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.80202438_80202446dup , CM000666.2:g.80202438_80202446dup	GRCh38
NC_000004.11:g.81123592_81123600dup , CM000666.1:g.81123592_81123600dup	GRCh37
NC_000004.10:g.81342616_81342624dup	NCBI36
NG_046725.1:g.22169_22177dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415738.3:c.976_984dup MANE Select	ENSP00000406998.2:p.Gly328_Leu329insGlyAlaGly
ENST00000339711.8:c.976_984dup	ENSP00000339764.4:p.Gly328_Leu329insGlyAlaGly
ENST00000415738.2:c.976_984dup	ENSP00000406998.2:p.Gly328_Leu329insGlyAlaGly
ENST00000504452.5:c.976_984dup	ENSP00000423985.1:p.Gly328_Leu329insGlyAlaGly
ENST00000515013.5:c.976_984dup	ENSP00000425149.1:p.Gly328_Leu329insGlyAlaGly
NM_001099403.1:c.976_984dup	NP_001092873.1:p.Gly328_Leu329insGlyAlaGly
NM_020226.3:c.976_984dup	NP_064611.3:p.Gly328_Leu329insGlyAlaGly
XM_005263144.2:c.979_987dup	XP_005263201.1:p.Gly329_Leu330insGlyAlaGly
XM_005263145.2:c.979_987dup	XP_005263202.1:p.Gly329_Leu330insGlyAlaGly
XM_005263146.3:c.976_984dup	XP_005263203.1:p.Gly328_Leu329insGlyAlaGly
XM_011532133.1:c.1819_1827dup	XP_011530435.1:p.Gly609_Leu610insGlyAlaGly
XM_011532134.1:c.1816_1824dup	XP_011530436.1:p.Gly608_Leu609insGlyAlaGly
XM_011532135.1:c.1678_1686dup	XP_011530437.1:p.Gly562_Leu563insGlyAlaGly
XM_011532136.1:c.1531_1539dup	XP_011530438.1:p.Gly513_Leu514insGlyAlaGly
XM_011532137.1:c.1531_1539dup	XP_011530439.1:p.Gly513_Leu514insGlyAlaGly
XM_011532138.1:c.1531_1539dup	XP_011530440.1:p.Gly513_Leu514insGlyAlaGly
XM_011532139.1:c.1531_1539dup	XP_011530441.1:p.Gly513_Leu514insGlyAlaGly
XM_011532140.1:c.1531_1539dup	XP_011530442.1:p.Gly513_Leu514insGlyAlaGly
XM_011532141.1:c.1393_1401dup	XP_011530443.1:p.Gly467_Leu468insGlyAlaGly
XM_011532142.1:c.1372_1380dup	XP_011530444.1:p.Gly460_Leu461insGlyAlaGly
XM_005263146.4:c.976_984dup	XP_005263203.1:p.Gly328_Leu329insGlyAlaGly
XM_011532133.2:c.1819_1827dup	XP_011530435.1:p.Gly609_Leu610insGlyAlaGly
XM_011532135.2:c.1678_1686dup	XP_011530437.1:p.Gly562_Leu563insGlyAlaGly
XM_011532140.2:c.1531_1539dup	XP_011530442.1:p.Gly513_Leu514insGlyAlaGly
XM_011532141.3:c.1393_1401dup	XP_011530443.1:p.Gly467_Leu468insGlyAlaGly
XM_017008468.1:c.1528_1536dup	XP_016863957.1:p.Gly512_Leu513insGlyAlaGly
XM_017008469.1:c.1615_1623dup	XP_016863958.1:p.Gly541_Leu542insGlyAlaGly
XM_017008470.1:c.1531_1539dup	XP_016863959.1:p.Gly513_Leu514insGlyAlaGly
NM_001099403.2:c.976_984dup MANE Select	NP_001092873.1:p.Gly328_Leu329insGlyAlaGly
NM_020226.4:c.976_984dup	NP_064611.3:p.Gly328_Leu329insGlyAlaGly