Canonical Allele Identifier: CA14495443

Gene: SLFN12L SLFN13

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.35516493T>G , CM000679.2:g.35516493T>G	GRCh38
NC_000017.10:g.33843512T>G , CM000679.1:g.33843512T>G	GRCh37
NC_000017.9:g.30867625T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000628453.4:c.86+5786A>C (SLFN12L) MANE Select	ENSP00000487397.4:n.86+5786A>C
ENST00000361112.6:c.101+5786A>C (SLFN12L)	ENSP00000354412.4:n.101+5786A>C
NM_001363830.1:c.101+5786A>C (SLFN12L)	NP_001350759.1:n.101+5786A>C
XM_017024006.1:c.-2188-1172A>C (SLFN12L)	XP_016879495.1:n.-2188-1172A>C
XM_017024007.1:c.-1590+5786A>C (SLFN12L)	XP_016879496.1:n.-1590+5786A>C
XM_024450521.1:c.-304+5786A>C (SLFN12L)	XP_024306289.1:n.-304+5786A>C
XM_024450522.1:c.-234+5786A>C (SLFN12L)	XP_024306290.1:n.-234+5786A>C
XM_024450523.1:c.-1995-1172A>C (SLFN12L)	XP_024306291.1:n.-1995-1172A>C
XM_024450616.1:c.-1735+5786A>C (SLFN13)	XP_024306384.1:n.-1735+5786A>C
NM_001195790.3:c.-288+5786A>C (SLFN12L)	NP_001182719.2:n.-288+5786A>C
NM_001363830.2:c.86+5786A>C (SLFN12L) MANE Select	NP_001350759.2:n.86+5786A>C