Canonical Allele Identifier: CA1323324911
Gene: FASTKD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.206767481_206767484delinsAAGG , CM000664.2:g.206767481_206767484delinsAAGG GRCh38
NC_000002.11:g.207632205_207632208delinsAAGG , CM000664.1:g.207632205_207632208delinsAAGG GRCh37
NC_000002.10:g.207340450_207340453delinsAAGG NCBI36
NG_008984.1:g.7094_7097delinsAAGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000402774.8:c.777+11_777+14delinsAAGG MANE Select ENSP00000385990.3:n.777+11_777+14delinsAAGG
ENST00000236980.10:c.777+11_777+14delinsAAGG ENSP00000236980.6:n.777+11_777+14delinsAAGG
ENST00000402774.7:c.777+11_777+14delinsAAGG ENSP00000385990.3:n.777+11_777+14delinsAAGG
ENST00000403094.3:c.777+11_777+14delinsAAGG ENSP00000384929.3:n.777+11_777+14delinsAAGG
ENST00000487777.5:n.835+11_835+14delinsAAGG
NM_001136193.1:c.777+11_777+14delinsAAGG NP_001129665.1:n.777+11_777+14delinsAAGG
NM_001136194.1:c.777+11_777+14delinsAAGG NP_001129666.1:n.777+11_777+14delinsAAGG
NM_014929.3:c.777+11_777+14delinsAAGG NP_055744.2:n.777+11_777+14delinsAAGG
NM_001136193.2:c.777+11_777+14delinsAAGG MANE Select NP_001129665.1:n.777+11_777+14delinsAAGG
NM_001136194.2:c.777+11_777+14delinsAAGG NP_001129666.1:n.777+11_777+14delinsAAGG
NM_014929.4:c.777+11_777+14delinsAAGG NP_055744.2:n.777+11_777+14delinsAAGG