Canonical Allele Identifier: CA527602076

Gene: FASLG

Linked Data

• dbSNP Id: rs1489624212
• gnomAD v2: 1-172634683-CCA-C
• gnomAD v3: 1-172665543-CCA-C
• gnomAD v4: 1-172665543-CCA-C
• MyVariant Identifiers: chr1:g.172634684_172634685del (hg19) ; chr1:g.172665544_172665545del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.172665546_172665547del , CM000663.2:g.172665546_172665547del	GRCh38
NC_000001.10:g.172634686_172634687del , CM000663.1:g.172634686_172634687del	GRCh37
NC_000001.9:g.170901309_170901310del	NCBI36
NG_007269.1:g.11502_11503del , LRG_58:g.11502_11503del

Transcript Alleles

HGVS	Amino-acid change
ENST00000367721.3:c.452-76_452-75del MANE Select	ENSP00000356694.2:n.452-76_452-75del
ENST00000340030.4:c.*22-76_*22-75del	ENSP00000344739.3:n.*22-76_*22-75del
ENST00000367721.2:c.452-76_452-75del	ENSP00000356694.2:n.452-76_452-75del
NM_000639.2:c.452-76_452-75del	NP_000630.1:n.452-76_452-75del
NM_001302746.1:c.*22-76_*22-75del	NP_001289675.1:n.*22-76_*22-75del
NM_000639.3:c.452-76_452-75del MANE Select	NP_000630.1:n.452-76_452-75del
NM_001302746.2:c.*22-76_*22-75del	NP_001289675.1:n.*22-76_*22-75del