Canonical Allele Identifier: CA527602097
Gene: FASLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.172659391_172659414dup , CM000663.2:g.172659391_172659414dup GRCh38
NC_000001.10:g.172628531_172628554dup , CM000663.1:g.172628531_172628554dup GRCh37
NC_000001.9:g.170895154_170895177dup NCBI36
NG_007269.1:g.5347_5370dup , LRG_58:g.5347_5370dup

Transcript Alleles

HGVS Amino-acid Change
NM_000639.3:c.190_213dup MANE Select NP_000630.1:p.Leu71_Lys72insProProLeuProLeuProProLeu
ENST00000367721.3:c.190_213dup MANE Select ENSP00000356694.2:p.Leu71_Lys72insProProLeuProLeuProProLeu
NM_000639.2:c.190_213dup NP_000630.1:p.Leu71_Lys72insProProLeuProLeuProProLeu
NM_001302746.1:c.190_213dup NP_001289675.1:p.Leu71_Lys72insProProLeuProLeuProProLeu
NM_001302746.2:c.190_213dup NP_001289675.1:p.Leu71_Lys72insProProLeuProLeuProProLeu
ENST00000340030.4:c.190_213dup ENSP00000344739.3:p.Leu71_Lys72insProProLeuProLeuProProLeu
ENST00000367721.2:c.190_213dup ENSP00000356694.2:p.Leu71_Lys72insProProLeuProLeuProProLeu