Canonical Allele Identifier: CA323871

Gene: FASTKD2

Linked Data

• ClinVar Variation Id: 214343
• ClinVar RCV Id: RCV000199343
• dbSNP Id: rs863223961
• MyVariant Identifiers: chr2:g.207631678T>A (hg19) ; chr2:g.206766954T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.206766954T>A , CM000664.2:g.206766954T>A	GRCh38
NC_000002.11:g.207631678T>A , CM000664.1:g.207631678T>A	GRCh37
NC_000002.10:g.207339923T>A	NCBI36
NG_008984.1:g.6567T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402774.8:c.261T>A MANE Select	ENSP00000385990.3:p.Asp87Glu
ENST00000236980.10:c.261T>A	ENSP00000236980.6:p.Asp87Glu
ENST00000402774.7:c.261T>A	ENSP00000385990.3:p.Asp87Glu
ENST00000403094.3:c.261T>A	ENSP00000384929.3:p.Asp87Glu
ENST00000418289.1:c.261T>A	ENSP00000409927.1:p.Asp87Glu
ENST00000487777.5:n.319T>A
NM_001136193.1:c.261T>A	NP_001129665.1:p.Asp87Glu
NM_001136194.1:c.261T>A	NP_001129666.1:p.Asp87Glu
NM_014929.3:c.261T>A	NP_055744.2:p.Asp87Glu
NM_001136193.2:c.261T>A MANE Select	NP_001129665.1:p.Asp87Glu
NM_001136194.2:c.261T>A	NP_001129666.1:p.Asp87Glu
NM_014929.4:c.261T>A	NP_055744.2:p.Asp87Glu