Canonical Allele Identifier: CA356536783

Gene: SEPSECS

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000382103.7:c.989G>C MANE Select	ENSP00000371535.2:p.Gly330Ala
ENST00000680581.1:c.989G>C	ENSP00000506483.1:p.Gly330Ala
ENST00000680824.1:n.2205G>C
ENST00000681071.1:n.1281G>C
ENST00000681341.1:n.2130G>C
ENST00000681948.1:c.1244G>C	ENSP00000505991.1:p.Gly415Ala
ENST00000358971.7:c.*787G>C	ENSP00000351857.3:n.*787G>C
ENST00000382103.6:c.989G>C	ENSP00000371535.2:p.Gly330Ala
ENST00000503150.1:c.271G>C
ENST00000505513.1:n.289G>C
ENST00000514585.5:c.*690G>C	ENSP00000421880.1:n.*690G>C
NM_016955.3:c.989G>C	NP_058651.3:p.Gly330Ala
XM_005248168.2:c.752G>C	XP_005248225.1:p.Gly251Ala
XM_006713965.2:c.809G>C	XP_006714028.1:p.Gly270Ala
XM_011513846.1:c.986G>C	XP_011512148.1:p.Gly329Ala
XM_011513847.1:c.956G>C	XP_011512149.1:p.Gly319Ala
XM_011513848.1:c.809G>C	XP_011512150.1:p.Gly270Ala
XM_011513846.2:c.986G>C	XP_011512148.1:p.Gly329Ala
XM_011513847.2:c.956G>C	XP_011512149.1:p.Gly319Ala
XM_017008277.1:c.1244G>C	XP_016863766.1:p.Gly415Ala
XM_017008278.1:c.566G>C	XP_016863767.1:p.Gly189Ala
NM_016955.4:c.989G>C MANE Select	NP_058651.3:p.Gly330Ala