Canonical Allele Identifier: CA356536629

Gene: SEPSECS

Linked Data

• MyVariant Identifiers: chr4:g.25146400C>A (hg19) ; chr4:g.25144778C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25144778C>A , CM000666.2:g.25144778C>A	GRCh38
NC_000004.11:g.25146400C>A , CM000666.1:g.25146400C>A	GRCh37
NC_000004.10:g.24755498C>A	NCBI36
NG_028222.1:g.20805G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.1022G>T MANE Select	ENSP00000371535.2:p.Arg341Ile
ENST00000680581.1:c.1022G>T	ENSP00000506483.1:p.Arg341Ile
ENST00000680824.1:n.2238G>T
ENST00000681071.1:n.1314G>T
ENST00000681341.1:n.2163G>T
ENST00000681948.1:c.1277G>T	ENSP00000505991.1:p.Arg426Ile
ENST00000358971.7:c.*820G>T	ENSP00000351857.3:n.*820G>T
ENST00000382103.6:c.1022G>T	ENSP00000371535.2:p.Arg341Ile
ENST00000503150.1:c.304G>T
ENST00000505513.1:n.322G>T
ENST00000514585.5:c.*723G>T	ENSP00000421880.1:n.*723G>T
NM_016955.3:c.1022G>T	NP_058651.3:p.Arg341Ile
XM_005248168.2:c.785G>T	XP_005248225.1:p.Arg262Ile
XM_006713965.2:c.842G>T	XP_006714028.1:p.Arg281Ile
XM_011513846.1:c.1019G>T	XP_011512148.1:p.Arg340Ile
XM_011513847.1:c.989G>T	XP_011512149.1:p.Arg330Ile
XM_011513848.1:c.842G>T	XP_011512150.1:p.Arg281Ile
XM_011513846.2:c.1019G>T	XP_011512148.1:p.Arg340Ile
XM_011513847.2:c.989G>T	XP_011512149.1:p.Arg330Ile
XM_017008277.1:c.1277G>T	XP_016863766.1:p.Arg426Ile
XM_017008278.1:c.599G>T	XP_016863767.1:p.Arg200Ile
NM_016955.4:c.1022G>T MANE Select	NP_058651.3:p.Arg341Ile