Canonical Allele Identifier: CA356536999

Gene: SEPSECS

Linked Data

• MyVariant Identifiers: chr4:g.25146488C>G (hg19) ; chr4:g.25144866C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25144866C>G , CM000666.2:g.25144866C>G	GRCh38
NC_000004.11:g.25146488C>G , CM000666.1:g.25146488C>G	GRCh37
NC_000004.10:g.24755586C>G	NCBI36
NG_028222.1:g.20717G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.935-1G>C MANE Select	ENSP00000371535.2:n.935-1G>C
ENST00000680581.1:c.935-1G>C	ENSP00000506483.1:n.935-1G>C
ENST00000680824.1:n.2151-1G>C
ENST00000681071.1:n.1227-1G>C
ENST00000681341.1:n.2076-1G>C
ENST00000681948.1:c.1190-1G>C	ENSP00000505991.1:n.1190-1G>C
ENST00000358971.7:c.*733-1G>C	ENSP00000351857.3:n.*733-1G>C
ENST00000382103.6:c.935-1G>C	ENSP00000371535.2:n.935-1G>C
ENST00000503150.1:c.217-1G>C
ENST00000505513.1:n.235-1G>C
ENST00000514585.5:c.*636-1G>C	ENSP00000421880.1:n.*636-1G>C
NM_016955.3:c.935-1G>C	NP_058651.3:n.935-1G>C
XM_005248168.2:c.698-1G>C	XP_005248225.1:n.698-1G>C
XM_006713965.2:c.755-1G>C	XP_006714028.1:n.755-1G>C
XM_011513846.1:c.932-1G>C	XP_011512148.1:n.932-1G>C
XM_011513847.1:c.902-1G>C	XP_011512149.1:n.902-1G>C
XM_011513848.1:c.755-1G>C	XP_011512150.1:n.755-1G>C
XM_011513846.2:c.932-1G>C	XP_011512148.1:n.932-1G>C
XM_011513847.2:c.902-1G>C	XP_011512149.1:n.902-1G>C
XM_017008277.1:c.1190-1G>C	XP_016863766.1:n.1190-1G>C
XM_017008278.1:c.512-1G>C	XP_016863767.1:n.512-1G>C
NM_016955.4:c.935-1G>C MANE Select	NP_058651.3:n.935-1G>C