Canonical Allele Identifier: CA2607292733

Gene: FASTKD2

Linked Data

• gnomAD v3: 2-206767642-A-AG
• gnomAD v4: 2-206767642-A-AG

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.206767642_206767643insG , CM000664.2:g.206767642_206767643insG	GRCh38
NC_000002.11:g.207632366_207632367insG , CM000664.1:g.207632366_207632367insG	GRCh37
NC_000002.10:g.207340611_207340612insG	NCBI36
NG_008984.1:g.7255_7256insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402774.8:c.777+172_777+173insG MANE Select	ENSP00000385990.3:n.777+172_777+173insG
ENST00000236980.10:c.777+172_777+173insG	ENSP00000236980.6:n.777+172_777+173insG
ENST00000402774.7:c.777+172_777+173insG	ENSP00000385990.3:n.777+172_777+173insG
ENST00000403094.3:c.777+172_777+173insG	ENSP00000384929.3:n.777+172_777+173insG
ENST00000487777.5:n.835+172_835+173insG
NM_001136193.1:c.777+172_777+173insG	NP_001129665.1:n.777+172_777+173insG
NM_001136194.1:c.777+172_777+173insG	NP_001129666.1:n.777+172_777+173insG
NM_014929.3:c.777+172_777+173insG	NP_055744.2:n.777+172_777+173insG
NM_001136193.2:c.777+172_777+173insG MANE Select	NP_001129665.1:n.777+172_777+173insG
NM_001136194.2:c.777+172_777+173insG	NP_001129666.1:n.777+172_777+173insG
NM_014929.4:c.777+172_777+173insG	NP_055744.2:n.777+172_777+173insG