Canonical Allele Identifier: CA1486839226

Gene: NDST4

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.115036437T= , CM000666.2:g.115036437T=	GRCh38
NC_000004.11:g.115957593T= , CM000666.1:g.115957593T=	GRCh37
NC_000004.10:g.116177042T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264363.7:c.978+39622A= MANE Select	ENSP00000264363.2:n.978+39622A=
ENST00000264363.6:c.978+39622A=	ENSP00000264363.2:n.978+39622A=
ENST00000504854.1:c.-71-65853A=	ENSP00000423218.1:n.-71-65853A=
ENST00000514570.1:n.407-59163A=
ENST00000613194.4:c.-160+39622A=	ENSP00000483949.1:n.-160+39622A=
NM_022569.1:c.978+39622A=	NP_072091.1:n.978+39622A=
NM_022569.2:c.978+39622A=	NP_072091.1:n.978+39622A=
XM_017008545.2:c.-159-59163A=	XP_016864034.1:n.-159-59163A=
XM_017008546.1:c.-72+39622A=	XP_016864035.1:n.-72+39622A=
NM_022569.3:c.978+39622A= MANE Select	NP_072091.1:n.978+39622A=