Canonical Allele Identifier: CA2663032619
Gene: SMARCAL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.216415501_216415517del , CM000664.2:g.216415501_216415517del GRCh38
NC_000002.11:g.217280224_217280240del , CM000664.1:g.217280224_217280240del GRCh37
NC_000002.10:g.216988469_216988485del NCBI36
NG_009771.1:g.8088_8104del , LRG_108:g.8088_8104del

Transcript Alleles

HGVS Amino-acid Change
ENST00000425815.6:c.797_811+2del
ENST00000430374.6:c.797_811+2del
ENST00000444508.6:c.797_811+2del
ENST00000697898.1:n.1158_1172+2del
ENST00000697899.1:c.797_811+2del
ENST00000697900.1:n.1073_1087+2del
ENST00000697901.1:c.797_811+2del
ENST00000697902.1:n.1029_1043+2del
ENST00000697903.1:c.797_811+2del
ENST00000697904.1:c.797_811+2del
ENST00000697905.1:c.797_811+2del
ENST00000697906.1:c.797_811+2del
ENST00000697907.1:c.797_811+2del
ENST00000357276.9:c.797_811+2del
ENST00000357276.8:c.797_811+2del
ENST00000358207.9:c.797_811+2del
ENST00000392128.6:c.389_403+2del
ENST00000427645.5:c.494_508+2del
NM_001127207.1:c.797_811+2del
NM_014140.3:c.797_811+2del , LRG_108t1:c.797_811+2del
XM_005246631.2:c.797_811+2del
XM_005246632.1:c.797_811+2del
XM_006712557.1:c.797_811+2del
XM_005246632.2:c.797_811+2del
XM_017004228.2:c.-120_-106+2del
NM_001127207.2:c.797_811+2del
NM_014140.4:c.797_811+2del