Canonical Allele Identifier: CA793319845

Gene: SEPSECS

Linked Data

• dbSNP Id: rs1460613640
• MyVariant Identifiers: chr4:g.25145909C>G (hg19) ; chr4:g.25144287C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25144287C>G , CM000666.2:g.25144287C>G	GRCh38
NC_000004.11:g.25145909C>G , CM000666.1:g.25145909C>G	GRCh37
NC_000004.10:g.24755007C>G	NCBI36
NG_028222.1:g.21296G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.1026+487G>C MANE Select	ENSP00000371535.2:n.1026+487G>C
ENST00000680581.1:c.1026+487G>C	ENSP00000506483.1:n.1026+487G>C
ENST00000680824.1:n.2242+487G>C
ENST00000681071.1:n.1318+487G>C
ENST00000681341.1:n.2167+487G>C
ENST00000681948.1:c.1281+487G>C	ENSP00000505991.1:n.1281+487G>C
ENST00000358971.7:c.*824+487G>C	ENSP00000351857.3:n.*824+487G>C
ENST00000382103.6:c.1026+487G>C	ENSP00000371535.2:n.1026+487G>C
ENST00000503150.1:c.308+487G>C
ENST00000505513.1:n.326+487G>C
ENST00000514585.5:c.*727+487G>C	ENSP00000421880.1:n.*727+487G>C
NM_016955.3:c.1026+487G>C	NP_058651.3:n.1026+487G>C
XM_005248168.2:c.789+487G>C	XP_005248225.1:n.789+487G>C
XM_006713965.2:c.846+487G>C	XP_006714028.1:n.846+487G>C
XM_011513846.1:c.1023+487G>C	XP_011512148.1:n.1023+487G>C
XM_011513847.1:c.993+487G>C	XP_011512149.1:n.993+487G>C
XM_011513848.1:c.846+487G>C	XP_011512150.1:n.846+487G>C
XM_011513846.2:c.1023+487G>C	XP_011512148.1:n.1023+487G>C
XM_011513847.2:c.993+487G>C	XP_011512149.1:n.993+487G>C
XM_017008277.1:c.1281+487G>C	XP_016863766.1:n.1281+487G>C
XM_017008278.1:c.603+487G>C	XP_016863767.1:n.603+487G>C
NM_016955.4:c.1026+487G>C MANE Select	NP_058651.3:n.1026+487G>C