Canonical Allele Identifier: CA350498024
Gene: SMARCAL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.216415479A>G , CM000664.2:g.216415479A>G GRCh38
NC_000002.11:g.217280202A>G , CM000664.1:g.217280202A>G GRCh37
NC_000002.10:g.216988447A>G NCBI36
NG_009771.1:g.8066A>G , LRG_108:g.8066A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000425815.6:c.775A>G ENSP00000394410.2:p.Ile259Val
ENST00000430374.6:c.775A>G ENSP00000405077.2:p.Ile259Val
ENST00000444508.6:c.775A>G ENSP00000398969.2:p.Ile259Val
ENST00000697898.1:n.1136A>G
ENST00000697899.1:c.775A>G ENSP00000513470.1:p.Ile259Val
ENST00000697900.1:n.1051A>G
ENST00000697901.1:c.775A>G ENSP00000513471.1:p.Ile259Val
ENST00000697902.1:n.1007A>G
ENST00000697903.1:c.775A>G ENSP00000513472.1:p.Ile259Val
ENST00000697904.1:c.775A>G ENSP00000513473.1:p.Ile259Val
ENST00000697905.1:c.775A>G ENSP00000513474.1:p.Ile259Val
ENST00000697906.1:c.775A>G ENSP00000513475.1:p.Ile259Val
ENST00000697907.1:c.775A>G ENSP00000513476.1:p.Ile259Val
ENST00000357276.9:c.775A>G MANE Select ENSP00000349823.4:p.Ile259Val
ENST00000357276.8:c.775A>G ENSP00000349823.4:p.Ile259Val
ENST00000358207.9:c.775A>G ENSP00000350940.5:p.Ile259Val
ENST00000392128.6:c.367A>G ENSP00000375974.2:p.Ile123Val
ENST00000427645.5:c.472A>G ENSP00000392997.1:p.Ile158Val
NM_001127207.1:c.775A>G NP_001120679.1:p.Ile259Val
NM_014140.3:c.775A>G , LRG_108t1:c.775A>G NP_054859.2:p.Ile259Val
XM_005246631.2:c.775A>G XP_005246688.1:p.Ile259Val
XM_005246632.1:c.775A>G XP_005246689.1:p.Ile259Val
XM_006712557.1:c.775A>G XP_006712620.1:p.Ile259Val
XM_005246632.2:c.775A>G XP_005246689.1:p.Ile259Val
XM_017004228.2:c.-142A>G XP_016859717.1:n.-142A>G
NM_001127207.2:c.775A>G NP_001120679.1:p.Ile259Val
NM_014140.4:c.775A>G MANE Select NP_054859.2:p.Ile259Val