Canonical Allele Identifier: CA356542888

Gene: SEPSECS

Linked Data

• MyVariant Identifiers: chr4:g.25158591A>C (hg19) ; chr4:g.25156969A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25156969A>C , CM000666.2:g.25156969A>C	GRCh38
NC_000004.11:g.25158591A>C , CM000666.1:g.25158591A>C	GRCh37
NC_000004.10:g.24767689A>C	NCBI36
NG_028222.1:g.8614T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.275T>G MANE Select	ENSP00000371535.2:p.Ile92Ser
ENST00000680581.1:c.275T>G	ENSP00000506483.1:p.Ile92Ser
ENST00000680824.1:n.1491T>G
ENST00000681071.1:n.567T>G
ENST00000681166.1:n.1322T>G
ENST00000681341.1:n.1416T>G
ENST00000681640.1:n.369T>G
ENST00000681948.1:c.530T>G	ENSP00000505991.1:p.Ile177Ser
ENST00000358971.7:c.*73T>G	ENSP00000351857.3:n.*73T>G
ENST00000382103.6:c.275T>G	ENSP00000371535.2:p.Ile92Ser
ENST00000514585.5:c.120T>G	ENSP00000421880.1:p.His40Gln
NM_016955.3:c.275T>G	NP_058651.3:p.Ile92Ser
XM_005248168.2:c.38T>G	XP_005248225.1:p.Ile13Ser
XM_006713965.2:c.95T>G	XP_006714028.1:p.Ile32Ser
XM_011513846.1:c.272T>G	XP_011512148.1:p.Ile91Ser
XM_011513847.1:c.242T>G	XP_011512149.1:p.Ile81Ser
XM_011513848.1:c.95T>G	XP_011512150.1:p.Ile32Ser
XM_011513846.2:c.272T>G	XP_011512148.1:p.Ile91Ser
XM_011513847.2:c.242T>G	XP_011512149.1:p.Ile81Ser
XM_017008277.1:c.530T>G	XP_016863766.1:p.Ile177Ser
XM_017008278.1:c.-149T>G	XP_016863767.1:n.-149T>G
NM_016955.4:c.275T>G MANE Select	NP_058651.3:p.Ile92Ser