Canonical Allele Identifier: CA2572679471

Gene: FASTKD2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.206767639_206767642dup , CM000664.2:g.206767639_206767642dup	GRCh38
NC_000002.11:g.207632363_207632366dup , CM000664.1:g.207632363_207632366dup	GRCh37
NC_000002.10:g.207340608_207340611dup	NCBI36
NG_008984.1:g.7252_7255dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402774.8:c.777+169_777+172dup MANE Select	ENSP00000385990.3:n.777+169_777+172dup
ENST00000236980.10:c.777+169_777+172dup	ENSP00000236980.6:n.777+169_777+172dup
ENST00000402774.7:c.777+169_777+172dup	ENSP00000385990.3:n.777+169_777+172dup
ENST00000403094.3:c.777+169_777+172dup	ENSP00000384929.3:n.777+169_777+172dup
ENST00000487777.5:n.835+169_835+172dup
NM_001136193.1:c.777+169_777+172dup	NP_001129665.1:n.777+169_777+172dup
NM_001136194.1:c.777+169_777+172dup	NP_001129666.1:n.777+169_777+172dup
NM_014929.3:c.777+169_777+172dup	NP_055744.2:n.777+169_777+172dup
NM_001136193.2:c.777+169_777+172dup MANE Select	NP_001129665.1:n.777+169_777+172dup
NM_001136194.2:c.777+169_777+172dup	NP_001129666.1:n.777+169_777+172dup
NM_014929.4:c.777+169_777+172dup	NP_055744.2:n.777+169_777+172dup