Canonical Allele Identifier: CA2662829196

Gene: FASTKD2

Linked Data

• gnomAD v4: 2-206767556-TAA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.206767559_206767560del , CM000664.2:g.206767559_206767560del	GRCh38
NC_000002.11:g.207632283_207632284del , CM000664.1:g.207632283_207632284del	GRCh37
NC_000002.10:g.207340528_207340529del	NCBI36
NG_008984.1:g.7172_7173del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402774.8:c.777+89_777+90del MANE Select	ENSP00000385990.3:n.777+89_777+90del
ENST00000236980.10:c.777+89_777+90del	ENSP00000236980.6:n.777+89_777+90del
ENST00000402774.7:c.777+89_777+90del	ENSP00000385990.3:n.777+89_777+90del
ENST00000403094.3:c.777+89_777+90del	ENSP00000384929.3:n.777+89_777+90del
ENST00000487777.5:n.835+89_835+90del
NM_001136193.1:c.777+89_777+90del	NP_001129665.1:n.777+89_777+90del
NM_001136194.1:c.777+89_777+90del	NP_001129666.1:n.777+89_777+90del
NM_014929.3:c.777+89_777+90del	NP_055744.2:n.777+89_777+90del
NM_001136193.2:c.777+89_777+90del MANE Select	NP_001129665.1:n.777+89_777+90del
NM_001136194.2:c.777+89_777+90del	NP_001129666.1:n.777+89_777+90del
NM_014929.4:c.777+89_777+90del	NP_055744.2:n.777+89_777+90del