Canonical Allele Identifier: CA1590995834

Gene: NDST1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150541574C= , CM000667.2:g.150541574C=	GRCh38
NC_000005.9:g.149921136C= , CM000667.1:g.149921136C=	GRCh37
NC_000005.8:g.149901329C=	NCBI36
NG_041806.1:g.48797C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261797.7:c.1754C= MANE Select	ENSP00000261797.6:p.Pro585=
ENST00000261797.6:c.1754C=	ENSP00000261797.6:p.Pro585=
ENST00000523767.5:c.1754C=	ENSP00000428604.1:p.Pro585=
NM_001301063.1:c.1754C=	NP_001287992.1:p.Pro585=
NM_001543.4:c.1754C=	NP_001534.1:p.Pro585=
XM_005268433.1:c.1754C=	XP_005268490.1:p.Pro585=
XM_005268434.1:c.1754C=	XP_005268491.1:p.Pro585=
XM_005268435.3:c.1754C=	XP_005268492.1:p.Pro585=
XM_005268436.2:c.1754C=	XP_005268493.1:p.Pro585=
XM_005268437.3:c.1754C=	XP_005268494.1:p.Pro585=
XM_005268438.1:c.1754C=	XP_005268495.1:p.Pro585=
XM_005268439.1:c.1754C=	XP_005268496.1:p.Pro585=
XM_005268442.2:c.482C=	XP_005268499.1:p.Pro161=
XM_006714782.1:c.1754C=	XP_006714845.1:p.Pro585=
XM_006714783.1:c.1754C=	XP_006714846.1:p.Pro585=
XM_011537638.1:c.767C=	XP_011535940.1:p.Pro256=
XR_245854.1:n.2232C=
XM_005268434.2:c.1754C=	XP_005268491.1:p.Pro585=
XM_005268435.4:c.1754C=	XP_005268492.1:p.Pro585=
XM_005268436.3:c.1754C=	XP_005268493.1:p.Pro585=
XM_005268437.5:c.1754C=	XP_005268494.1:p.Pro585=
XM_005268442.4:c.482C=	XP_005268499.1:p.Pro161=
XM_006714782.2:c.1754C=	XP_006714845.1:p.Pro585=
XM_011537638.2:c.767C=	XP_011535940.1:p.Pro256=
XM_017009427.1:c.1754C=	XP_016864916.1:p.Pro585=
XM_017009428.1:c.1754C=	XP_016864917.1:p.Pro585=
XM_017009429.2:c.1754C=	XP_016864918.1:p.Pro585=
XM_017009430.2:c.1754C=	XP_016864919.1:p.Pro585=
XM_017009431.1:c.1754C=	XP_016864920.1:p.Pro585=
XM_017009432.1:c.767C=	XP_016864921.1:p.Pro256=
XM_017009433.1:c.767C=	XP_016864922.1:p.Pro256=
XR_001742060.2:n.2262C=
XR_001742061.1:n.2851C=
XR_245854.2:n.2232C=
NM_001543.5:c.1754C= MANE Select	NP_001534.1:p.Pro585=
NM_001301063.2:c.1754C=	NP_001287992.1:p.Pro585=