Canonical Allele Identifier: CA2662829199

Gene: FASTKD2

Linked Data

• gnomAD v4: 2-206767565-CTA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.206767567_206767568del , CM000664.2:g.206767567_206767568del	GRCh38
NC_000002.11:g.207632291_207632292del , CM000664.1:g.207632291_207632292del	GRCh37
NC_000002.10:g.207340536_207340537del	NCBI36
NG_008984.1:g.7180_7181del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402774.8:c.777+97_777+98del MANE Select	ENSP00000385990.3:n.777+97_777+98del
ENST00000236980.10:c.777+97_777+98del	ENSP00000236980.6:n.777+97_777+98del
ENST00000402774.7:c.777+97_777+98del	ENSP00000385990.3:n.777+97_777+98del
ENST00000403094.3:c.777+97_777+98del	ENSP00000384929.3:n.777+97_777+98del
ENST00000487777.5:n.835+97_835+98del
NM_001136193.1:c.777+97_777+98del	NP_001129665.1:n.777+97_777+98del
NM_001136194.1:c.777+97_777+98del	NP_001129666.1:n.777+97_777+98del
NM_014929.3:c.777+97_777+98del	NP_055744.2:n.777+97_777+98del
NM_001136193.2:c.777+97_777+98del MANE Select	NP_001129665.1:n.777+97_777+98del
NM_001136194.2:c.777+97_777+98del	NP_001129666.1:n.777+97_777+98del
NM_014929.4:c.777+97_777+98del	NP_055744.2:n.777+97_777+98del