Canonical Allele Identifier: CA421944433

Gene: FASLG

Linked Data

• MyVariant Identifiers: chr1:g.172634820G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.172665680G>T , CM000663.2:g.172665680G>T	GRCh38
NC_000001.10:g.172634820G>T , CM000663.1:g.172634820G>T	GRCh37
NC_000001.9:g.170901443G>T	NCBI36
NG_007269.1:g.11636G>T , LRG_58:g.11636G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367721.3:c.510G>T MANE Select	ENSP00000356694.2:p.Leu170=
ENST00000340030.4:c.*80G>T	ENSP00000344739.3:n.*80G>T
ENST00000367721.2:c.510G>T	ENSP00000356694.2:p.Leu170=
NM_000639.2:c.510G>T	NP_000630.1:p.Leu170=
NM_001302746.1:c.*80G>T	NP_001289675.1:n.*80G>T
NM_000639.3:c.510G>T MANE Select	NP_000630.1:p.Leu170=
NM_001302746.2:c.*80G>T	NP_001289675.1:n.*80G>T