Canonical Allele Identifier: CA763821839

Gene: FASTKD2

Linked Data

• dbSNP Id: rs1285894477
• MyVariant Identifiers: chr2:g.207632408A>T (hg19) ; chr2:g.206767684A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.206767684A>T , CM000664.2:g.206767684A>T	GRCh38
NC_000002.11:g.207632408A>T , CM000664.1:g.207632408A>T	GRCh37
NC_000002.10:g.207340653A>T	NCBI36
NG_008984.1:g.7297A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402774.8:c.777+214A>T MANE Select	ENSP00000385990.3:n.777+214A>T
ENST00000236980.10:c.777+214A>T	ENSP00000236980.6:n.777+214A>T
ENST00000402774.7:c.777+214A>T	ENSP00000385990.3:n.777+214A>T
ENST00000403094.3:c.777+214A>T	ENSP00000384929.3:n.777+214A>T
ENST00000487777.5:n.835+214A>T
NM_001136193.1:c.777+214A>T	NP_001129665.1:n.777+214A>T
NM_001136194.1:c.777+214A>T	NP_001129666.1:n.777+214A>T
NM_014929.3:c.777+214A>T	NP_055744.2:n.777+214A>T
NM_001136193.2:c.777+214A>T MANE Select	NP_001129665.1:n.777+214A>T
NM_001136194.2:c.777+214A>T	NP_001129666.1:n.777+214A>T
NM_014929.4:c.777+214A>T	NP_055744.2:n.777+214A>T