Canonical Allele Identifier: CA1207431050
Gene: FASLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.172664137_172664138delinsTA , CM000663.2:g.172664137_172664138delinsTA GRCh38
NC_000001.10:g.172633277_172633278delinsTA , CM000663.1:g.172633277_172633278delinsTA GRCh37
NC_000001.9:g.170899900_170899901delinsTA NCBI36
NG_007269.1:g.10093_10094delinsTA , LRG_58:g.10093_10094delinsTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000367721.3:c.395-197_395-196delinsTA MANE Select ENSP00000356694.2:n.395-197_395-196delinsTA
ENST00000340030.4:c.349-197_349-196delinsTA ENSP00000344739.3:n.349-197_349-196delinsTA
ENST00000367721.2:c.395-197_395-196delinsTA ENSP00000356694.2:n.395-197_395-196delinsTA
NM_000639.2:c.395-197_395-196delinsTA NP_000630.1:n.395-197_395-196delinsTA
NM_001302746.1:c.349-197_349-196delinsTA NP_001289675.1:n.349-197_349-196delinsTA
NM_000639.3:c.395-197_395-196delinsTA MANE Select NP_000630.1:n.395-197_395-196delinsTA
NM_001302746.2:c.349-197_349-196delinsTA NP_001289675.1:n.349-197_349-196delinsTA