Canonical Allele Identifier: CA438732698

Gene: SEPSECS

Linked Data

• MyVariant Identifiers: chr4:g.25158482C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25156860C>G , CM000666.2:g.25156860C>G	GRCh38
NC_000004.11:g.25158482C>G , CM000666.1:g.25158482C>G	GRCh37
NC_000004.10:g.24767580C>G	NCBI36
NG_028222.1:g.8723G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000382103.7:c.384G>C MANE Select	ENSP00000371535.2:p.Leu128=
ENST00000680581.1:c.384G>C	ENSP00000506483.1:p.Leu128=
ENST00000680824.1:n.1600G>C
ENST00000681071.1:n.676G>C
ENST00000681166.1:n.1431G>C
ENST00000681341.1:n.1525G>C
ENST00000681640.1:n.478G>C
ENST00000681948.1:c.639G>C	ENSP00000505991.1:p.Leu213=
ENST00000358971.7:c.*182G>C	ENSP00000351857.3:n.*182G>C
ENST00000382103.6:c.384G>C	ENSP00000371535.2:p.Leu128=
ENST00000514585.5:c.*85G>C	ENSP00000421880.1:n.*85G>C
NM_016955.3:c.384G>C	NP_058651.3:p.Leu128=
XM_005248168.2:c.147G>C	XP_005248225.1:p.Leu49=
XM_006713965.2:c.204G>C	XP_006714028.1:p.Leu68=
XM_011513846.1:c.381G>C	XP_011512148.1:p.Leu127=
XM_011513847.1:c.351G>C	XP_011512149.1:p.Leu117=
XM_011513848.1:c.204G>C	XP_011512150.1:p.Leu68=
XM_011513846.2:c.381G>C	XP_011512148.1:p.Leu127=
XM_011513847.2:c.351G>C	XP_011512149.1:p.Leu117=
XM_017008277.1:c.639G>C	XP_016863766.1:p.Leu213=
XM_017008278.1:c.-40G>C	XP_016863767.1:n.-40G>C
NM_016955.4:c.384G>C MANE Select	NP_058651.3:p.Leu128=