Canonical Allele Identifier: CA356536766

Gene: SEPSECS

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000382103.7:c.994A>T MANE Select	ENSP00000371535.2:p.Asn332Tyr
ENST00000680581.1:c.994A>T	ENSP00000506483.1:p.Asn332Tyr
ENST00000680824.1:n.2210A>T
ENST00000681071.1:n.1286A>T
ENST00000681341.1:n.2135A>T
ENST00000681948.1:c.1249A>T	ENSP00000505991.1:p.Asn417Tyr
ENST00000358971.7:c.*792A>T	ENSP00000351857.3:n.*792A>T
ENST00000382103.6:c.994A>T	ENSP00000371535.2:p.Asn332Tyr
ENST00000503150.1:c.276A>T
ENST00000505513.1:n.294A>T
ENST00000514585.5:c.*695A>T	ENSP00000421880.1:n.*695A>T
NM_016955.3:c.994A>T	NP_058651.3:p.Asn332Tyr
XM_005248168.2:c.757A>T	XP_005248225.1:p.Asn253Tyr
XM_006713965.2:c.814A>T	XP_006714028.1:p.Asn272Tyr
XM_011513846.1:c.991A>T	XP_011512148.1:p.Asn331Tyr
XM_011513847.1:c.961A>T	XP_011512149.1:p.Asn321Tyr
XM_011513848.1:c.814A>T	XP_011512150.1:p.Asn272Tyr
XM_011513846.2:c.991A>T	XP_011512148.1:p.Asn331Tyr
XM_011513847.2:c.961A>T	XP_011512149.1:p.Asn321Tyr
XM_017008277.1:c.1249A>T	XP_016863766.1:p.Asn417Tyr
XM_017008278.1:c.571A>T	XP_016863767.1:p.Asn191Tyr
NM_016955.4:c.994A>T MANE Select	NP_058651.3:p.Asn332Tyr