Canonical Allele Identifier: CA2655997607
Gene: GAS2L1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.29312727C>G , CM000684.2:g.29312727C>G GRCh38
NC_000022.10:g.29708716C>G , CM000684.1:g.29708716C>G GRCh37
NC_000022.9:g.28038716C>G NCBI36
NG_032959.1:g.10721C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000616432.5:c.*230C>G MANE Select ENSP00000478908.1:n.*230C>G
ENST00000406549.7:c.*230C>G ENSP00000383995.3:n.*230C>G
ENST00000611648.2:c.*230C>G ENSP00000479551.1:n.*230C>G
ENST00000616432.4:c.*230C>G ENSP00000478908.1:n.*230C>G
ENST00000618518.3:c.*230C>G ENSP00000481012.1:n.*230C>G
ENST00000621062.4:c.*230C>G ENSP00000478343.1:n.*230C>G
NM_001278730.1:c.*230C>G NP_001265659.1:n.*230C>G
NM_006478.4:c.*230C>G NP_006469.2:n.*230C>G
NM_152236.2:c.*230C>G NP_689422.1:n.*230C>G
XM_011529824.1:c.*230C>G XP_011528126.1:n.*230C>G
XM_011529825.1:c.*230C>G XP_011528127.1:n.*230C>G
NM_001362985.1:c.*230C>G NP_001349914.1:n.*230C>G
XM_017028533.1:c.*230C>G XP_016884022.1:n.*230C>G
NM_001278730.2:c.*230C>G NP_001265659.1:n.*230C>G
NM_001362985.2:c.*230C>G NP_001349914.1:n.*230C>G
NM_006478.5:c.*230C>G NP_006469.2:n.*230C>G
NM_152236.3:c.*230C>G NP_689422.1:n.*230C>G
NM_001362985.3:c.*230C>G MANE Select NP_001349914.1:n.*230C>G
NM_001395196.1:c.*230C>G NP_001382125.1:n.*230C>G
NM_001395197.1:c.*230C>G NP_001382126.1:n.*230C>G