Canonical Allele Identifier: CA356536769

Gene: SEPSECS

Linked Data

• MyVariant Identifiers: chr4:g.25146428T>G (hg19) ; chr4:g.25144806T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25144806T>G , CM000666.2:g.25144806T>G	GRCh38
NC_000004.11:g.25146428T>G , CM000666.1:g.25146428T>G	GRCh37
NC_000004.10:g.24755526T>G	NCBI36
NG_028222.1:g.20777A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000382103.7:c.994A>C MANE Select	ENSP00000371535.2:p.Asn332His
ENST00000680581.1:c.994A>C	ENSP00000506483.1:p.Asn332His
ENST00000680824.1:n.2210A>C
ENST00000681071.1:n.1286A>C
ENST00000681341.1:n.2135A>C
ENST00000681948.1:c.1249A>C	ENSP00000505991.1:p.Asn417His
ENST00000358971.7:c.*792A>C	ENSP00000351857.3:n.*792A>C
ENST00000382103.6:c.994A>C	ENSP00000371535.2:p.Asn332His
ENST00000503150.1:c.276A>C
ENST00000505513.1:n.294A>C
ENST00000514585.5:c.*695A>C	ENSP00000421880.1:n.*695A>C
NM_016955.3:c.994A>C	NP_058651.3:p.Asn332His
XM_005248168.2:c.757A>C	XP_005248225.1:p.Asn253His
XM_006713965.2:c.814A>C	XP_006714028.1:p.Asn272His
XM_011513846.1:c.991A>C	XP_011512148.1:p.Asn331His
XM_011513847.1:c.961A>C	XP_011512149.1:p.Asn321His
XM_011513848.1:c.814A>C	XP_011512150.1:p.Asn272His
XM_011513846.2:c.991A>C	XP_011512148.1:p.Asn331His
XM_011513847.2:c.961A>C	XP_011512149.1:p.Asn321His
XM_017008277.1:c.1249A>C	XP_016863766.1:p.Asn417His
XM_017008278.1:c.571A>C	XP_016863767.1:p.Asn191His
NM_016955.4:c.994A>C MANE Select	NP_058651.3:p.Asn332His