Canonical Allele Identifier: CA2578454362

Gene: NDST1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150541563_150541564del , CM000667.2:g.150541563_150541564del	GRCh38
NC_000005.9:g.149921125_149921126del , CM000667.1:g.149921125_149921126del	GRCh37
NC_000005.8:g.149901318_149901319del	NCBI36
NG_041806.1:g.48786_48787del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261797.7:c.1750-7_1750-6del MANE Select	ENSP00000261797.6:n.1750-7_1750-6del
ENST00000261797.6:c.1750-7_1750-6del	ENSP00000261797.6:n.1750-7_1750-6del
ENST00000523767.5:c.1750-7_1750-6del	ENSP00000428604.1:n.1750-7_1750-6del
NM_001301063.1:c.1750-7_1750-6del	NP_001287992.1:n.1750-7_1750-6del
NM_001543.4:c.1750-7_1750-6del	NP_001534.1:n.1750-7_1750-6del
XM_005268433.1:c.1750-7_1750-6del	XP_005268490.1:n.1750-7_1750-6del
XM_005268434.1:c.1750-7_1750-6del	XP_005268491.1:n.1750-7_1750-6del
XM_005268435.3:c.1750-7_1750-6del	XP_005268492.1:n.1750-7_1750-6del
XM_005268436.2:c.1750-7_1750-6del	XP_005268493.1:n.1750-7_1750-6del
XM_005268437.3:c.1750-7_1750-6del	XP_005268494.1:n.1750-7_1750-6del
XM_005268438.1:c.1750-7_1750-6del	XP_005268495.1:n.1750-7_1750-6del
XM_005268439.1:c.1750-7_1750-6del	XP_005268496.1:n.1750-7_1750-6del
XM_005268442.2:c.478-7_478-6del	XP_005268499.1:n.478-7_478-6del
XM_006714782.1:c.1750-7_1750-6del	XP_006714845.1:n.1750-7_1750-6del
XM_006714783.1:c.1750-7_1750-6del	XP_006714846.1:n.1750-7_1750-6del
XM_011537638.1:c.763-7_763-6del	XP_011535940.1:n.763-7_763-6del
XR_245854.1:n.2228-7_2228-6del
XM_005268434.2:c.1750-7_1750-6del	XP_005268491.1:n.1750-7_1750-6del
XM_005268435.4:c.1750-7_1750-6del	XP_005268492.1:n.1750-7_1750-6del
XM_005268436.3:c.1750-7_1750-6del	XP_005268493.1:n.1750-7_1750-6del
XM_005268437.5:c.1750-7_1750-6del	XP_005268494.1:n.1750-7_1750-6del
XM_005268442.4:c.478-7_478-6del	XP_005268499.1:n.478-7_478-6del
XM_006714782.2:c.1750-7_1750-6del	XP_006714845.1:n.1750-7_1750-6del
XM_011537638.2:c.763-7_763-6del	XP_011535940.1:n.763-7_763-6del
XM_017009427.1:c.1750-7_1750-6del	XP_016864916.1:n.1750-7_1750-6del
XM_017009428.1:c.1750-7_1750-6del	XP_016864917.1:n.1750-7_1750-6del
XM_017009429.2:c.1750-7_1750-6del	XP_016864918.1:n.1750-7_1750-6del
XM_017009430.2:c.1750-7_1750-6del	XP_016864919.1:n.1750-7_1750-6del
XM_017009431.1:c.1750-7_1750-6del	XP_016864920.1:n.1750-7_1750-6del
XM_017009432.1:c.763-7_763-6del	XP_016864921.1:n.763-7_763-6del
XM_017009433.1:c.763-7_763-6del	XP_016864922.1:n.763-7_763-6del
XR_001742060.2:n.2258-7_2258-6del
XR_001742061.1:n.2847-7_2847-6del
XR_245854.2:n.2228-7_2228-6del
NM_001543.5:c.1750-7_1750-6del MANE Select	NP_001534.1:n.1750-7_1750-6del
NM_001301063.2:c.1750-7_1750-6del	NP_001287992.1:n.1750-7_1750-6del