Canonical Allele Identifier: CA438732340

Gene: SEPSECS

Linked Data

• MyVariant Identifiers: chr4:g.25146486T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25144864T>A , CM000666.2:g.25144864T>A	GRCh38
NC_000004.11:g.25146486T>A , CM000666.1:g.25146486T>A	GRCh37
NC_000004.10:g.24755584T>A	NCBI36
NG_028222.1:g.20719A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.936A>T MANE Select	ENSP00000371535.2:p.Gly312=
ENST00000680581.1:c.936A>T	ENSP00000506483.1:p.Gly312=
ENST00000680824.1:n.2152A>T
ENST00000681071.1:n.1228A>T
ENST00000681341.1:n.2077A>T
ENST00000681948.1:c.1191A>T	ENSP00000505991.1:p.Gly397=
ENST00000358971.7:c.*734A>T	ENSP00000351857.3:n.*734A>T
ENST00000382103.6:c.936A>T	ENSP00000371535.2:p.Gly312=
ENST00000503150.1:c.218A>T
ENST00000505513.1:n.236A>T
ENST00000514585.5:c.*637A>T	ENSP00000421880.1:n.*637A>T
NM_016955.3:c.936A>T	NP_058651.3:p.Gly312=
XM_005248168.2:c.699A>T	XP_005248225.1:p.Gly233=
XM_006713965.2:c.756A>T	XP_006714028.1:p.Gly252=
XM_011513846.1:c.933A>T	XP_011512148.1:p.Gly311=
XM_011513847.1:c.903A>T	XP_011512149.1:p.Gly301=
XM_011513848.1:c.756A>T	XP_011512150.1:p.Gly252=
XM_011513846.2:c.933A>T	XP_011512148.1:p.Gly311=
XM_011513847.2:c.903A>T	XP_011512149.1:p.Gly301=
XM_017008277.1:c.1191A>T	XP_016863766.1:p.Gly397=
XM_017008278.1:c.513A>T	XP_016863767.1:p.Gly171=
NM_016955.4:c.936A>T MANE Select	NP_058651.3:p.Gly312=