Canonical Allele Identifier: CA1323324942
Gene: FASTKD2 HGNC NCBI

Linked Data

dbSNP Id: rs1689558283

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.206767563_206767564del , CM000664.2:g.206767563_206767564del GRCh38
NC_000002.11:g.207632287_207632288del , CM000664.1:g.207632287_207632288del GRCh37
NC_000002.10:g.207340532_207340533del NCBI36
NG_008984.1:g.7176_7177del

Transcript Alleles

HGVS Amino-acid Change
ENST00000402774.8:c.777+93_777+94del MANE Select ENSP00000385990.3:n.777+93_777+94del
ENST00000236980.10:c.777+93_777+94del ENSP00000236980.6:n.777+93_777+94del
ENST00000402774.7:c.777+93_777+94del ENSP00000385990.3:n.777+93_777+94del
ENST00000403094.3:c.777+93_777+94del ENSP00000384929.3:n.777+93_777+94del
ENST00000487777.5:n.835+93_835+94del
NM_001136193.1:c.777+93_777+94del NP_001129665.1:n.777+93_777+94del
NM_001136194.1:c.777+93_777+94del NP_001129666.1:n.777+93_777+94del
NM_014929.3:c.777+93_777+94del NP_055744.2:n.777+93_777+94del
NM_001136193.2:c.777+93_777+94del MANE Select NP_001129665.1:n.777+93_777+94del
NM_001136194.2:c.777+93_777+94del NP_001129666.1:n.777+93_777+94del
NM_014929.4:c.777+93_777+94del NP_055744.2:n.777+93_777+94del