Canonical Allele Identifier: CA1327821409
Gene: SMARCAL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.216415215A= , CM000664.2:g.216415215A= GRCh38
NC_000002.11:g.217279938A= , CM000664.1:g.217279938A= GRCh37
NC_000002.10:g.216988183A= NCBI36
NG_009771.1:g.7802A= , LRG_108:g.7802A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000425815.6:c.511A= ENSP00000394410.2:p.Lys171=
ENST00000430374.6:c.511A= ENSP00000405077.2:p.Lys171=
ENST00000444508.6:c.511A= ENSP00000398969.2:p.Lys171=
ENST00000697898.1:n.872A=
ENST00000697899.1:c.511A= ENSP00000513470.1:p.Lys171=
ENST00000697900.1:n.787A=
ENST00000697901.1:c.511A= ENSP00000513471.1:p.Lys171=
ENST00000697902.1:n.743A=
ENST00000697903.1:c.511A= ENSP00000513472.1:p.Lys171=
ENST00000697904.1:c.511A= ENSP00000513473.1:p.Lys171=
ENST00000697905.1:c.511A= ENSP00000513474.1:p.Lys171=
ENST00000697906.1:c.511A= ENSP00000513475.1:p.Lys171=
ENST00000697907.1:c.511A= ENSP00000513476.1:p.Lys171=
ENST00000357276.9:c.511A= MANE Select ENSP00000349823.4:p.Lys171=
ENST00000357276.8:c.511A= ENSP00000349823.4:p.Lys171=
ENST00000358207.9:c.511A= ENSP00000350940.5:p.Lys171=
ENST00000392128.6:c.103A= ENSP00000375974.2:p.Lys35=
ENST00000427645.5:c.208A= ENSP00000392997.1:p.Lys70=
NM_001127207.1:c.511A= NP_001120679.1:p.Lys171=
NM_014140.3:c.511A= , LRG_108t1:c.511A= NP_054859.2:p.Lys171=
XM_005246631.2:c.511A= XP_005246688.1:p.Lys171=
XM_005246632.1:c.511A= XP_005246689.1:p.Lys171=
XM_006712557.1:c.511A= XP_006712620.1:p.Lys171=
XM_005246632.2:c.511A= XP_005246689.1:p.Lys171=
XM_017004228.2:c.-406A= XP_016859717.1:n.-406A=
NM_001127207.2:c.511A= NP_001120679.1:p.Lys171=
NM_014140.4:c.511A= MANE Select NP_054859.2:p.Lys171=