Canonical Allele Identifier: CA350070893

Gene: FASTKD2

Linked Data

• gnomAD v4: 2-206767130-C-G
• MyVariant Identifiers: chr2:g.207631854C>G (hg19) ; chr2:g.206767130C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.206767130C>G , CM000664.2:g.206767130C>G	GRCh38
NC_000002.11:g.207631854C>G , CM000664.1:g.207631854C>G	GRCh37
NC_000002.10:g.207340099C>G	NCBI36
NG_008984.1:g.6743C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402774.8:c.437C>G MANE Select	ENSP00000385990.3:p.Thr146Ser
ENST00000236980.10:c.437C>G	ENSP00000236980.6:p.Thr146Ser
ENST00000402774.7:c.437C>G	ENSP00000385990.3:p.Thr146Ser
ENST00000403094.3:c.437C>G	ENSP00000384929.3:p.Thr146Ser
ENST00000487777.5:n.495C>G
NM_001136193.1:c.437C>G	NP_001129665.1:p.Thr146Ser
NM_001136194.1:c.437C>G	NP_001129666.1:p.Thr146Ser
NM_014929.3:c.437C>G	NP_055744.2:p.Thr146Ser
NM_001136193.2:c.437C>G MANE Select	NP_001129665.1:p.Thr146Ser
NM_001136194.2:c.437C>G	NP_001129666.1:p.Thr146Ser
NM_014929.4:c.437C>G	NP_055744.2:p.Thr146Ser