Canonical Allele Identifier: CA103861349
Gene: NDST4 HGNC NCBI

Linked Data

dbSNP Id: rs13150562

Genomic Alleles

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

Transcript Alleles

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