Canonical Allele Identifier: CA438732775

Gene: SEPSECS

Linked Data

• MyVariant Identifiers: chr4:g.25158590A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25156968A>G , CM000666.2:g.25156968A>G	GRCh38
NC_000004.11:g.25158590A>G , CM000666.1:g.25158590A>G	GRCh37
NC_000004.10:g.24767688A>G	NCBI36
NG_028222.1:g.8615T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.276T>C MANE Select	ENSP00000371535.2:p.Ile92=
ENST00000680581.1:c.276T>C	ENSP00000506483.1:p.Ile92=
ENST00000680824.1:n.1492T>C
ENST00000681071.1:n.568T>C
ENST00000681166.1:n.1323T>C
ENST00000681341.1:n.1417T>C
ENST00000681640.1:n.370T>C
ENST00000681948.1:c.531T>C	ENSP00000505991.1:p.Ile177=
ENST00000358971.7:c.*74T>C	ENSP00000351857.3:n.*74T>C
ENST00000382103.6:c.276T>C	ENSP00000371535.2:p.Ile92=
ENST00000514585.5:c.121T>C	ENSP00000421880.1:p.Ser41Pro
NM_016955.3:c.276T>C	NP_058651.3:p.Ile92=
XM_005248168.2:c.39T>C	XP_005248225.1:p.Ile13=
XM_006713965.2:c.96T>C	XP_006714028.1:p.Ile32=
XM_011513846.1:c.273T>C	XP_011512148.1:p.Ile91=
XM_011513847.1:c.243T>C	XP_011512149.1:p.Ile81=
XM_011513848.1:c.96T>C	XP_011512150.1:p.Ile32=
XM_011513846.2:c.273T>C	XP_011512148.1:p.Ile91=
XM_011513847.2:c.243T>C	XP_011512149.1:p.Ile81=
XM_017008277.1:c.531T>C	XP_016863766.1:p.Ile177=
XM_017008278.1:c.-148T>C	XP_016863767.1:n.-148T>C
NM_016955.4:c.276T>C MANE Select	NP_058651.3:p.Ile92=