Canonical Allele Identifier: CA431114896
Gene: FASTKD2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.207632104T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.206767380T>C , CM000664.2:g.206767380T>C GRCh38
NC_000002.11:g.207632104T>C , CM000664.1:g.207632104T>C GRCh37
NC_000002.10:g.207340349T>C NCBI36
NG_008984.1:g.6993T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000402774.8:c.687T>C MANE Select ENSP00000385990.3:p.Tyr229=
ENST00000236980.10:c.687T>C ENSP00000236980.6:p.Tyr229=
ENST00000402774.7:c.687T>C ENSP00000385990.3:p.Tyr229=
ENST00000403094.3:c.687T>C ENSP00000384929.3:p.Tyr229=
ENST00000487777.5:n.745T>C
NM_001136193.1:c.687T>C NP_001129665.1:p.Tyr229=
NM_001136194.1:c.687T>C NP_001129666.1:p.Tyr229=
NM_014929.3:c.687T>C NP_055744.2:p.Tyr229=
NM_001136193.2:c.687T>C MANE Select NP_001129665.1:p.Tyr229=
NM_001136194.2:c.687T>C NP_001129666.1:p.Tyr229=
NM_014929.4:c.687T>C NP_055744.2:p.Tyr229=
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