Canonical Allele Identifier: CA1207431047

Gene: FASLG

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.172664133_172664138delinsGGTTTA , CM000663.2:g.172664133_172664138delinsGGTTTA	GRCh38
NC_000001.10:g.172633273_172633278delinsGGTTTA , CM000663.1:g.172633273_172633278delinsGGTTTA	GRCh37
NC_000001.9:g.170899896_170899901delinsGGTTTA	NCBI36
NG_007269.1:g.10089_10094delinsGGTTTA , LRG_58:g.10089_10094delinsGGTTTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367721.3:c.395-201_395-196delinsGGTTTA MANE Select	ENSP00000356694.2:n.395-201_395-196delinsGGTTTA
ENST00000340030.4:c.349-201_349-196delinsGGTTTA	ENSP00000344739.3:n.349-201_349-196delinsGGTTTA
ENST00000367721.2:c.395-201_395-196delinsGGTTTA	ENSP00000356694.2:n.395-201_395-196delinsGGTTTA
NM_000639.2:c.395-201_395-196delinsGGTTTA	NP_000630.1:n.395-201_395-196delinsGGTTTA
NM_001302746.1:c.349-201_349-196delinsGGTTTA	NP_001289675.1:n.349-201_349-196delinsGGTTTA
NM_000639.3:c.395-201_395-196delinsGGTTTA MANE Select	NP_000630.1:n.395-201_395-196delinsGGTTTA
NM_001302746.2:c.349-201_349-196delinsGGTTTA	NP_001289675.1:n.349-201_349-196delinsGGTTTA