Canonical Allele Identifier: CA361768167
Gene: NDST1 HGNC NCBI

Linked Data

dbSNP Id: rs1359429635

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000261797.7:c.1754C>T MANE Select ENSP00000261797.6:p.Pro585Leu
ENST00000261797.6:c.1754C>T ENSP00000261797.6:p.Pro585Leu
ENST00000523767.5:c.1754C>T ENSP00000428604.1:p.Pro585Leu
NM_001301063.1:c.1754C>T NP_001287992.1:p.Pro585Leu
NM_001543.4:c.1754C>T NP_001534.1:p.Pro585Leu
XM_005268433.1:c.1754C>T XP_005268490.1:p.Pro585Leu
XM_005268434.1:c.1754C>T XP_005268491.1:p.Pro585Leu
XM_005268435.3:c.1754C>T XP_005268492.1:p.Pro585Leu
XM_005268436.2:c.1754C>T XP_005268493.1:p.Pro585Leu
XM_005268437.3:c.1754C>T XP_005268494.1:p.Pro585Leu
XM_005268438.1:c.1754C>T XP_005268495.1:p.Pro585Leu
XM_005268439.1:c.1754C>T XP_005268496.1:p.Pro585Leu
XM_005268442.2:c.482C>T XP_005268499.1:p.Pro161Leu
XM_006714782.1:c.1754C>T XP_006714845.1:p.Pro585Leu
XM_006714783.1:c.1754C>T XP_006714846.1:p.Pro585Leu
XM_011537638.1:c.767C>T XP_011535940.1:p.Pro256Leu
XR_245854.1:n.2232C>T
XM_005268434.2:c.1754C>T XP_005268491.1:p.Pro585Leu
XM_005268435.4:c.1754C>T XP_005268492.1:p.Pro585Leu
XM_005268436.3:c.1754C>T XP_005268493.1:p.Pro585Leu
XM_005268437.5:c.1754C>T XP_005268494.1:p.Pro585Leu
XM_005268442.4:c.482C>T XP_005268499.1:p.Pro161Leu
XM_006714782.2:c.1754C>T XP_006714845.1:p.Pro585Leu
XM_011537638.2:c.767C>T XP_011535940.1:p.Pro256Leu
XM_017009427.1:c.1754C>T XP_016864916.1:p.Pro585Leu
XM_017009428.1:c.1754C>T XP_016864917.1:p.Pro585Leu
XM_017009429.2:c.1754C>T XP_016864918.1:p.Pro585Leu
XM_017009430.2:c.1754C>T XP_016864919.1:p.Pro585Leu
XM_017009431.1:c.1754C>T XP_016864920.1:p.Pro585Leu
XM_017009432.1:c.767C>T XP_016864921.1:p.Pro256Leu
XM_017009433.1:c.767C>T XP_016864922.1:p.Pro256Leu
XR_001742060.2:n.2262C>T
XR_001742061.1:n.2851C>T
XR_245854.2:n.2232C>T
NM_001543.5:c.1754C>T MANE Select NP_001534.1:p.Pro585Leu
NM_001301063.2:c.1754C>T NP_001287992.1:p.Pro585Leu