Canonical Allele Identifier: CA2818684127

Gene: GAS2L1

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29312723G>C , CM000684.2:g.29312723G>C	GRCh38
NC_000022.10:g.29708712G>C , CM000684.1:g.29708712G>C	GRCh37
NC_000022.9:g.28038712G>C	NCBI36
NG_032959.1:g.10717G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000616432.5:c.*226G>C MANE Select	ENSP00000478908.1:n.*226G>C
ENST00000406549.7:c.*226G>C	ENSP00000383995.3:n.*226G>C
ENST00000611648.2:c.*226G>C	ENSP00000479551.1:n.*226G>C
ENST00000616432.4:c.*226G>C	ENSP00000478908.1:n.*226G>C
ENST00000618518.3:c.*226G>C	ENSP00000481012.1:n.*226G>C
ENST00000621062.4:c.*226G>C	ENSP00000478343.1:n.*226G>C
NM_001278730.1:c.*226G>C	NP_001265659.1:n.*226G>C
NM_006478.4:c.*226G>C	NP_006469.2:n.*226G>C
NM_152236.2:c.*226G>C	NP_689422.1:n.*226G>C
XM_011529824.1:c.*226G>C	XP_011528126.1:n.*226G>C
XM_011529825.1:c.*226G>C	XP_011528127.1:n.*226G>C
NM_001362985.1:c.*226G>C	NP_001349914.1:n.*226G>C
XM_017028533.1:c.*226G>C	XP_016884022.1:n.*226G>C
NM_001278730.2:c.*226G>C	NP_001265659.1:n.*226G>C
NM_001362985.2:c.*226G>C	NP_001349914.1:n.*226G>C
NM_006478.5:c.*226G>C	NP_006469.2:n.*226G>C
NM_152236.3:c.*226G>C	NP_689422.1:n.*226G>C
NM_001362985.3:c.*226G>C MANE Select	NP_001349914.1:n.*226G>C
NM_001395196.1:c.*226G>C	NP_001382125.1:n.*226G>C
NM_001395197.1:c.*226G>C	NP_001382126.1:n.*226G>C