Canonical Allele Identifier: CA356536781

Gene: SEPSECS

Linked Data

• MyVariant Identifiers: chr4:g.25146433C>A (hg19) ; chr4:g.25144811C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25144811C>A , CM000666.2:g.25144811C>A	GRCh38
NC_000004.11:g.25146433C>A , CM000666.1:g.25146433C>A	GRCh37
NC_000004.10:g.24755531C>A	NCBI36
NG_028222.1:g.20772G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000382103.7:c.989G>T MANE Select	ENSP00000371535.2:p.Gly330Val
ENST00000680581.1:c.989G>T	ENSP00000506483.1:p.Gly330Val
ENST00000680824.1:n.2205G>T
ENST00000681071.1:n.1281G>T
ENST00000681341.1:n.2130G>T
ENST00000681948.1:c.1244G>T	ENSP00000505991.1:p.Gly415Val
ENST00000358971.7:c.*787G>T	ENSP00000351857.3:n.*787G>T
ENST00000382103.6:c.989G>T	ENSP00000371535.2:p.Gly330Val
ENST00000503150.1:c.271G>T
ENST00000505513.1:n.289G>T
ENST00000514585.5:c.*690G>T	ENSP00000421880.1:n.*690G>T
NM_016955.3:c.989G>T	NP_058651.3:p.Gly330Val
XM_005248168.2:c.752G>T	XP_005248225.1:p.Gly251Val
XM_006713965.2:c.809G>T	XP_006714028.1:p.Gly270Val
XM_011513846.1:c.986G>T	XP_011512148.1:p.Gly329Val
XM_011513847.1:c.956G>T	XP_011512149.1:p.Gly319Val
XM_011513848.1:c.809G>T	XP_011512150.1:p.Gly270Val
XM_011513846.2:c.986G>T	XP_011512148.1:p.Gly329Val
XM_011513847.2:c.956G>T	XP_011512149.1:p.Gly319Val
XM_017008277.1:c.1244G>T	XP_016863766.1:p.Gly415Val
XM_017008278.1:c.566G>T	XP_016863767.1:p.Gly189Val
NM_016955.4:c.989G>T MANE Select	NP_058651.3:p.Gly330Val