Canonical Allele Identifier: CA438732282

Gene: SEPSECS

Linked Data

• MyVariant Identifiers: chr4:g.25146410G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25144788G>A , CM000666.2:g.25144788G>A	GRCh38
NC_000004.11:g.25146410G>A , CM000666.1:g.25146410G>A	GRCh37
NC_000004.10:g.24755508G>A	NCBI36
NG_028222.1:g.20795C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.1012C>T MANE Select	ENSP00000371535.2:p.Leu338=
ENST00000680581.1:c.1012C>T	ENSP00000506483.1:p.Leu338=
ENST00000680824.1:n.2228C>T
ENST00000681071.1:n.1304C>T
ENST00000681341.1:n.2153C>T
ENST00000681948.1:c.1267C>T	ENSP00000505991.1:p.Leu423=
ENST00000358971.7:c.*810C>T	ENSP00000351857.3:n.*810C>T
ENST00000382103.6:c.1012C>T	ENSP00000371535.2:p.Leu338=
ENST00000503150.1:c.294C>T
ENST00000505513.1:n.312C>T
ENST00000514585.5:c.*713C>T	ENSP00000421880.1:n.*713C>T
NM_016955.3:c.1012C>T	NP_058651.3:p.Leu338=
XM_005248168.2:c.775C>T	XP_005248225.1:p.Leu259=
XM_006713965.2:c.832C>T	XP_006714028.1:p.Leu278=
XM_011513846.1:c.1009C>T	XP_011512148.1:p.Leu337=
XM_011513847.1:c.979C>T	XP_011512149.1:p.Leu327=
XM_011513848.1:c.832C>T	XP_011512150.1:p.Leu278=
XM_011513846.2:c.1009C>T	XP_011512148.1:p.Leu337=
XM_011513847.2:c.979C>T	XP_011512149.1:p.Leu327=
XM_017008277.1:c.1267C>T	XP_016863766.1:p.Leu423=
XM_017008278.1:c.589C>T	XP_016863767.1:p.Leu197=
NM_016955.4:c.1012C>T MANE Select	NP_058651.3:p.Leu338=