Canonical Allele Identifier: CA350069555

Gene: FASTKD2

Linked Data

• MyVariant Identifiers: chr2:g.207631710T>A (hg19) ; chr2:g.206766986T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.206766986T>A , CM000664.2:g.206766986T>A	GRCh38
NC_000002.11:g.207631710T>A , CM000664.1:g.207631710T>A	GRCh37
NC_000002.10:g.207339955T>A	NCBI36
NG_008984.1:g.6599T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402774.8:c.293T>A MANE Select	ENSP00000385990.3:p.Leu98Gln
ENST00000236980.10:c.293T>A	ENSP00000236980.6:p.Leu98Gln
ENST00000402774.7:c.293T>A	ENSP00000385990.3:p.Leu98Gln
ENST00000403094.3:c.293T>A	ENSP00000384929.3:p.Leu98Gln
ENST00000418289.1:c.293T>A	ENSP00000409927.1:p.Leu98Gln
ENST00000487777.5:n.351T>A
NM_001136193.1:c.293T>A	NP_001129665.1:p.Leu98Gln
NM_001136194.1:c.293T>A	NP_001129666.1:p.Leu98Gln
NM_014929.3:c.293T>A	NP_055744.2:p.Leu98Gln
NM_001136193.2:c.293T>A MANE Select	NP_001129665.1:p.Leu98Gln
NM_001136194.2:c.293T>A	NP_001129666.1:p.Leu98Gln
NM_014929.4:c.293T>A	NP_055744.2:p.Leu98Gln