Canonical Allele Identifier: CA362800250

Gene: JARID2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.15504590G>A , CM000668.2:g.15504590G>A	GRCh38
NC_000006.11:g.15504821G>A , CM000668.1:g.15504821G>A	GRCh37
NC_000006.10:g.15612800G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_004973.4:c.2539G>A MANE Select	NP_004964.2:p.Glu847Lys
ENST00000341776.7:c.2539G>A MANE Select	ENSP00000341280.2:p.Glu847Lys
NM_001267040.1:c.2023G>A	NP_001253969.1:p.Glu675Lys
NM_004973.3:c.2539G>A	NP_004964.2:p.Glu847Lys
ENST00000341776.6:c.2539G>A	ENSP00000341280.2:p.Glu847Lys
ENST00000397311.4:c.2023G>A	ENSP00000380478.3:p.Glu675Lys
ENST00000474854.1:n.143G>A
XM_005249089.2:c.2023G>A	XP_005249146.1:p.Glu675Lys
XM_011514578.1:c.2023G>A	XP_011512880.1:p.Glu675Lys
XM_011514579.1:c.2728G>A	XP_011512881.1:p.Glu910Lys
XM_011514579.3:c.2728G>A	XP_011512881.1:p.Glu910Lys
XM_011514580.1:c.2584G>A	XP_011512882.1:p.Glu862Lys
XM_011514581.1:c.2023G>A	XP_011512883.1:p.Glu675Lys
XM_011514582.1:c.2131G>A	XP_011512884.1:p.Glu711Lys
XM_011514583.1:c.2131G>A	XP_011512885.1:p.Glu711Lys
XM_011514584.1:c.2023G>A	XP_011512886.1:p.Glu675Lys
XM_017010833.2:c.2683G>A	XP_016866322.1:p.Glu895Lys
XM_017010834.2:c.2023G>A	XP_016866323.1:p.Glu675Lys
XM_017010835.2:c.2023G>A	XP_016866324.1:p.Glu675Lys
XM_024446424.1:c.2470G>A	XP_024302192.1:p.Glu824Lys
XM_024446425.1:c.2023G>A	XP_024302193.1:p.Glu675Lys