Canonical Allele Identifier: CA2147501831

Gene: JDP2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.75469814T= , CM000676.2:g.75469814T=	GRCh38
NC_000014.8:g.75936517T= , CM000676.1:g.75936517T=	GRCh37
NC_000014.7:g.75006270T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001135048.2:c.*339T= MANE Select	NP_001128520.1:n.*339T=
ENST00000651602.1:c.*339T= MANE Select	ENSP00000498745.1:n.*339T=
NM_001135047.1:c.*339T=	NP_001128519.1:n.*339T=
NM_001135047.2:c.*339T=	NP_001128519.1:n.*339T=
NM_001135048.1:c.*339T=	NP_001128520.1:n.*339T=
NM_001135049.1:c.*339T=	NP_001128521.1:n.*339T=
NM_130469.3:c.*339T=	NP_569736.1:n.*339T=
ENST00000267569.5:c.*339T=	ENSP00000267569.5:n.*339T=
ENST00000435893.6:c.*339T=	ENSP00000399587.2:n.*339T=
ENST00000437176.5:c.*339T=	ENSP00000409787.1:n.*339T=
XM_005267332.3:c.*339T=	XP_005267389.1:n.*339T=
XM_005267332.4:c.*339T=	XP_005267389.1:n.*339T=
XM_006720032.2:c.*339T=	XP_006720095.1:n.*339T=
XM_017020971.1:c.*339T=	XP_016876460.1:n.*339T=
XM_017020972.1:c.*339T=	XP_016876461.1:n.*339T=
XM_017020973.1:c.*339T=	XP_016876462.1:n.*339T=
XM_017020974.1:c.*339T=	XP_016876463.1:n.*339T=
XM_017020975.2:c.*339T=	XP_016876464.1:n.*339T=