Canonical Allele Identifier: CA2655997652
Gene: GAS2L1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.29312772del , CM000684.2:g.29312772del GRCh38
NC_000022.10:g.29708761del , CM000684.1:g.29708761del GRCh37
NC_000022.9:g.28038761del NCBI36
NG_032959.1:g.10766del

Transcript Alleles

HGVS Amino-acid Change
ENST00000616432.5:c.*275del MANE Select ENSP00000478908.1:n.*275del
ENST00000406549.7:c.*275del ENSP00000383995.3:n.*275del
ENST00000611648.2:c.*275del ENSP00000479551.1:n.*275del
ENST00000616432.4:c.*275del ENSP00000478908.1:n.*275del
ENST00000618518.3:c.*275del ENSP00000481012.1:n.*275del
ENST00000621062.4:c.*275del ENSP00000478343.1:n.*275del
NM_001278730.1:c.*275del NP_001265659.1:n.*275del
NM_006478.4:c.*275del NP_006469.2:n.*275del
NM_152236.2:c.*275del NP_689422.1:n.*275del
XM_011529824.1:c.*275del XP_011528126.1:n.*275del
XM_011529825.1:c.*275del XP_011528127.1:n.*275del
NM_001362985.1:c.*275del NP_001349914.1:n.*275del
XM_017028533.1:c.*275del XP_016884022.1:n.*275del
NM_001278730.2:c.*275del NP_001265659.1:n.*275del
NM_001362985.2:c.*275del NP_001349914.1:n.*275del
NM_006478.5:c.*275del NP_006469.2:n.*275del
NM_152236.3:c.*275del NP_689422.1:n.*275del
NM_001362985.3:c.*275del MANE Select NP_001349914.1:n.*275del
NM_001395196.1:c.*275del NP_001382125.1:n.*275del
NM_001395197.1:c.*275del NP_001382126.1:n.*275del