Canonical Allele Identifier: CA431114866
Gene: FASTKD2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.207632095C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.206767371C>A , CM000664.2:g.206767371C>A GRCh38
NC_000002.11:g.207632095C>A , CM000664.1:g.207632095C>A GRCh37
NC_000002.10:g.207340340C>A NCBI36
NG_008984.1:g.6984C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000402774.8:c.678C>A MANE Select ENSP00000385990.3:p.Ile226=
ENST00000236980.10:c.678C>A ENSP00000236980.6:p.Ile226=
ENST00000402774.7:c.678C>A ENSP00000385990.3:p.Ile226=
ENST00000403094.3:c.678C>A ENSP00000384929.3:p.Ile226=
ENST00000487777.5:n.736C>A
NM_001136193.1:c.678C>A NP_001129665.1:p.Ile226=
NM_001136194.1:c.678C>A NP_001129666.1:p.Ile226=
NM_014929.3:c.678C>A NP_055744.2:p.Ile226=
NM_001136193.2:c.678C>A MANE Select NP_001129665.1:p.Ile226=
NM_001136194.2:c.678C>A NP_001129666.1:p.Ile226=
NM_014929.4:c.678C>A NP_055744.2:p.Ile226=
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