Canonical Allele Identifier: CA350073168

Gene: FASTKD2

Linked Data

• MyVariant Identifiers: chr2:g.207632112T>C (hg19) ; chr2:g.206767388T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.206767388T>C , CM000664.2:g.206767388T>C	GRCh38
NC_000002.11:g.207632112T>C , CM000664.1:g.207632112T>C	GRCh37
NC_000002.10:g.207340357T>C	NCBI36
NG_008984.1:g.7001T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402774.8:c.695T>C MANE Select	ENSP00000385990.3:p.Leu232Pro
ENST00000236980.10:c.695T>C	ENSP00000236980.6:p.Leu232Pro
ENST00000402774.7:c.695T>C	ENSP00000385990.3:p.Leu232Pro
ENST00000403094.3:c.695T>C	ENSP00000384929.3:p.Leu232Pro
ENST00000487777.5:n.753T>C
NM_001136193.1:c.695T>C	NP_001129665.1:p.Leu232Pro
NM_001136194.1:c.695T>C	NP_001129666.1:p.Leu232Pro
NM_014929.3:c.695T>C	NP_055744.2:p.Leu232Pro
NM_001136193.2:c.695T>C MANE Select	NP_001129665.1:p.Leu232Pro
NM_001136194.2:c.695T>C	NP_001129666.1:p.Leu232Pro
NM_014929.4:c.695T>C	NP_055744.2:p.Leu232Pro