Canonical Allele Identifier: CA2276371465

Gene: SEC14L1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.77215126C= , CM000679.2:g.77215126C=	GRCh38
NC_000017.10:g.75211208C= , CM000679.1:g.75211208C=	GRCh37
NC_000017.9:g.72722803C=	NCBI36
NG_050640.1:g.131484C=
NG_050640.2:g.131484C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001143998.2:c.*1103C= MANE Select	NP_001137470.2:n.*1103C=
ENST00000436233.9:c.*1103C= MANE Select	ENSP00000390392.3:n.*1103C=
NM_001039573.2:c.2144+1107C=	NP_001034662.2:n.2144+1107C=
NM_001039573.3:c.2144+1107C=	NP_001034662.3:n.2144+1107C=
NM_001143998.1:c.*1103C=	NP_001137470.1:n.*1103C=
NM_001143999.1:c.*1103C=	NP_001137471.1:n.*1103C=
NM_001143999.2:c.*1103C=	NP_001137471.2:n.*1103C=
NM_001144001.1:c.*1103C=	NP_001137473.1:n.*1103C=
NM_001144001.2:c.*1103C=	NP_001137473.2:n.*1103C=
NM_001204408.1:c.2144+1107C=	NP_001191337.1:n.2144+1107C=
NM_001204408.2:c.2144+1107C=	NP_001191337.2:n.2144+1107C=
NM_001204410.1:c.*1103C=	NP_001191339.1:n.*1103C=
NM_001204410.2:c.*1103C=	NP_001191339.2:n.*1103C=
NM_003003.3:c.*1103C=	NP_002994.3:n.*1103C=
NM_003003.4:c.*1103C=	NP_002994.4:n.*1103C=
ENST00000392476.6:c.2144+1107C=	ENSP00000376268.2:n.2144+1107C=
ENST00000430767.8:c.*1103C=	ENSP00000408169.3:n.*1103C=
ENST00000436233.8:c.*1103C=	ENSP00000390392.3:n.*1103C=
ENST00000443798.8:c.2144+1107C=	ENSP00000406030.3:n.2144+1107C=