Canonical Allele Identifier: CA2503493037

Gene: GAS2L1

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29312648T>G , CM000684.2:g.29312648T>G	GRCh38
NC_000022.10:g.29708637T>G , CM000684.1:g.29708637T>G	GRCh37
NC_000022.9:g.28038637T>G	NCBI36
NG_032959.1:g.10642T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000616432.5:c.*151T>G MANE Select	ENSP00000478908.1:n.*151T>G
ENST00000406549.7:c.*151T>G	ENSP00000383995.3:n.*151T>G
ENST00000611648.2:c.*151T>G	ENSP00000479551.1:n.*151T>G
ENST00000616432.4:c.*151T>G	ENSP00000478908.1:n.*151T>G
ENST00000618518.3:c.*151T>G	ENSP00000481012.1:n.*151T>G
ENST00000621062.4:c.*151T>G	ENSP00000478343.1:n.*151T>G
NM_001278730.1:c.*151T>G	NP_001265659.1:n.*151T>G
NM_006478.4:c.*151T>G	NP_006469.2:n.*151T>G
NM_152236.2:c.*151T>G	NP_689422.1:n.*151T>G
XM_011529824.1:c.*151T>G	XP_011528126.1:n.*151T>G
XM_011529825.1:c.*151T>G	XP_011528127.1:n.*151T>G
NM_001362985.1:c.*151T>G	NP_001349914.1:n.*151T>G
XM_017028533.1:c.*151T>G	XP_016884022.1:n.*151T>G
NM_001278730.2:c.*151T>G	NP_001265659.1:n.*151T>G
NM_001362985.2:c.*151T>G	NP_001349914.1:n.*151T>G
NM_006478.5:c.*151T>G	NP_006469.2:n.*151T>G
NM_152236.3:c.*151T>G	NP_689422.1:n.*151T>G
NM_001362985.3:c.*151T>G MANE Select	NP_001349914.1:n.*151T>G
NM_001395196.1:c.*151T>G	NP_001382125.1:n.*151T>G
NM_001395197.1:c.*151T>G	NP_001382126.1:n.*151T>G