Canonical Allele Identifier: CA356542883

Gene: SEPSECS

Linked Data

• MyVariant Identifiers: chr4:g.25158590A>C (hg19) ; chr4:g.25156968A>C (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.276T>G MANE Select	ENSP00000371535.2:p.Ile92Met
ENST00000680581.1:c.276T>G	ENSP00000506483.1:p.Ile92Met
ENST00000680824.1:n.1492T>G
ENST00000681071.1:n.568T>G
ENST00000681166.1:n.1323T>G
ENST00000681341.1:n.1417T>G
ENST00000681640.1:n.370T>G
ENST00000681948.1:c.531T>G	ENSP00000505991.1:p.Ile177Met
ENST00000358971.7:c.*74T>G	ENSP00000351857.3:n.*74T>G
ENST00000382103.6:c.276T>G	ENSP00000371535.2:p.Ile92Met
ENST00000514585.5:c.121T>G	ENSP00000421880.1:p.Ser41Ala
NM_016955.3:c.276T>G	NP_058651.3:p.Ile92Met
XM_005248168.2:c.39T>G	XP_005248225.1:p.Ile13Met
XM_006713965.2:c.96T>G	XP_006714028.1:p.Ile32Met
XM_011513846.1:c.273T>G	XP_011512148.1:p.Ile91Met
XM_011513847.1:c.243T>G	XP_011512149.1:p.Ile81Met
XM_011513848.1:c.96T>G	XP_011512150.1:p.Ile32Met
XM_011513846.2:c.273T>G	XP_011512148.1:p.Ile91Met
XM_011513847.2:c.243T>G	XP_011512149.1:p.Ile81Met
XM_017008277.1:c.531T>G	XP_016863766.1:p.Ile177Met
XM_017008278.1:c.-148T>G	XP_016863767.1:n.-148T>G
NM_016955.4:c.276T>G MANE Select	NP_058651.3:p.Ile92Met