Canonical Allele Identifier: CA2540292544
Gene: SPTY2D1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.18611448del , CM000673.2:g.18611448del GRCh38
NC_000011.9:g.18632995del , CM000673.1:g.18632995del GRCh37
NC_000011.8:g.18589571del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000336349.6:c.1964+33del MANE Select ENSP00000337991.5:n.1964+33del
ENST00000336349.5:c.1964+33del ENSP00000337991.5:n.1964+33del
NM_194285.2:c.1964+33del NP_919261.2:n.1964+33del
XM_011519919.1:c.1712+33del XP_011518221.1:n.1712+33del
XM_011519919.2:c.1712+33del XP_011518221.1:n.1712+33del
NM_194285.3:c.1964+33del MANE Select NP_919261.2:n.1964+33del