Canonical Allele Identifier: CA356536720

Gene: SEPSECS

Linked Data

• MyVariant Identifiers: chr4:g.25146418T>A (hg19) ; chr4:g.25144796T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25144796T>A , CM000666.2:g.25144796T>A	GRCh38
NC_000004.11:g.25146418T>A , CM000666.1:g.25146418T>A	GRCh37
NC_000004.10:g.24755516T>A	NCBI36
NG_028222.1:g.20787A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.1004A>T MANE Select	ENSP00000371535.2:p.Lys335Met
ENST00000680581.1:c.1004A>T	ENSP00000506483.1:p.Lys335Met
ENST00000680824.1:n.2220A>T
ENST00000681071.1:n.1296A>T
ENST00000681341.1:n.2145A>T
ENST00000681948.1:c.1259A>T	ENSP00000505991.1:p.Lys420Met
ENST00000358971.7:c.*802A>T	ENSP00000351857.3:n.*802A>T
ENST00000382103.6:c.1004A>T	ENSP00000371535.2:p.Lys335Met
ENST00000503150.1:c.286A>T
ENST00000505513.1:n.304A>T
ENST00000514585.5:c.*705A>T	ENSP00000421880.1:n.*705A>T
NM_016955.3:c.1004A>T	NP_058651.3:p.Lys335Met
XM_005248168.2:c.767A>T	XP_005248225.1:p.Lys256Met
XM_006713965.2:c.824A>T	XP_006714028.1:p.Lys275Met
XM_011513846.1:c.1001A>T	XP_011512148.1:p.Lys334Met
XM_011513847.1:c.971A>T	XP_011512149.1:p.Lys324Met
XM_011513848.1:c.824A>T	XP_011512150.1:p.Lys275Met
XM_011513846.2:c.1001A>T	XP_011512148.1:p.Lys334Met
XM_011513847.2:c.971A>T	XP_011512149.1:p.Lys324Met
XM_017008277.1:c.1259A>T	XP_016863766.1:p.Lys420Met
XM_017008278.1:c.581A>T	XP_016863767.1:p.Lys194Met
NM_016955.4:c.1004A>T MANE Select	NP_058651.3:p.Lys335Met