Canonical Allele Identifier: CA1323324966

Gene: FASTKD2

Linked Data

• dbSNP Id: rs1689559457

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.206767611_206767614del , CM000664.2:g.206767611_206767614del	GRCh38
NC_000002.11:g.207632335_207632338del , CM000664.1:g.207632335_207632338del	GRCh37
NC_000002.10:g.207340580_207340583del	NCBI36
NG_008984.1:g.7224_7227del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402774.8:c.777+141_777+144del MANE Select	ENSP00000385990.3:n.777+141_777+144del
ENST00000236980.10:c.777+141_777+144del	ENSP00000236980.6:n.777+141_777+144del
ENST00000402774.7:c.777+141_777+144del	ENSP00000385990.3:n.777+141_777+144del
ENST00000403094.3:c.777+141_777+144del	ENSP00000384929.3:n.777+141_777+144del
ENST00000487777.5:n.835+141_835+144del
NM_001136193.1:c.777+141_777+144del	NP_001129665.1:n.777+141_777+144del
NM_001136194.1:c.777+141_777+144del	NP_001129666.1:n.777+141_777+144del
NM_014929.3:c.777+141_777+144del	NP_055744.2:n.777+141_777+144del
NM_001136193.2:c.777+141_777+144del MANE Select	NP_001129665.1:n.777+141_777+144del
NM_001136194.2:c.777+141_777+144del	NP_001129666.1:n.777+141_777+144del
NM_014929.4:c.777+141_777+144del	NP_055744.2:n.777+141_777+144del