Canonical Allele Identifier: CA2655997660

Gene: GAS2L1

Linked Data

• gnomAD v4: 22-29312774-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29312774T>C , CM000684.2:g.29312774T>C	GRCh38
NC_000022.10:g.29708763T>C , CM000684.1:g.29708763T>C	GRCh37
NC_000022.9:g.28038763T>C	NCBI36
NG_032959.1:g.10768T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000616432.5:c.*277T>C MANE Select	ENSP00000478908.1:n.*277T>C
ENST00000406549.7:c.*277T>C	ENSP00000383995.3:n.*277T>C
ENST00000611648.2:c.*277T>C	ENSP00000479551.1:n.*277T>C
ENST00000616432.4:c.*277T>C	ENSP00000478908.1:n.*277T>C
ENST00000618518.3:c.*277T>C	ENSP00000481012.1:n.*277T>C
ENST00000621062.4:c.*277T>C	ENSP00000478343.1:n.*277T>C
NM_001278730.1:c.*277T>C	NP_001265659.1:n.*277T>C
NM_006478.4:c.*277T>C	NP_006469.2:n.*277T>C
NM_152236.2:c.*277T>C	NP_689422.1:n.*277T>C
XM_011529824.1:c.*277T>C	XP_011528126.1:n.*277T>C
XM_011529825.1:c.*277T>C	XP_011528127.1:n.*277T>C
NM_001362985.1:c.*277T>C	NP_001349914.1:n.*277T>C
XM_017028533.1:c.*277T>C	XP_016884022.1:n.*277T>C
NM_001278730.2:c.*277T>C	NP_001265659.1:n.*277T>C
NM_001362985.2:c.*277T>C	NP_001349914.1:n.*277T>C
NM_006478.5:c.*277T>C	NP_006469.2:n.*277T>C
NM_152236.3:c.*277T>C	NP_689422.1:n.*277T>C
NM_001362985.3:c.*277T>C MANE Select	NP_001349914.1:n.*277T>C
NM_001395196.1:c.*277T>C	NP_001382125.1:n.*277T>C
NM_001395197.1:c.*277T>C	NP_001382126.1:n.*277T>C