Canonical Allele Identifier: CA356536764

Gene: SEPSECS

Linked Data

• MyVariant Identifiers: chr4:g.25146427T>G (hg19) ; chr4:g.25144805T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25144805T>G , CM000666.2:g.25144805T>G	GRCh38
NC_000004.11:g.25146427T>G , CM000666.1:g.25146427T>G	GRCh37
NC_000004.10:g.24755525T>G	NCBI36
NG_028222.1:g.20778A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000382103.7:c.995A>C MANE Select	ENSP00000371535.2:p.Asn332Thr
ENST00000680581.1:c.995A>C	ENSP00000506483.1:p.Asn332Thr
ENST00000680824.1:n.2211A>C
ENST00000681071.1:n.1287A>C
ENST00000681341.1:n.2136A>C
ENST00000681948.1:c.1250A>C	ENSP00000505991.1:p.Asn417Thr
ENST00000358971.7:c.*793A>C	ENSP00000351857.3:n.*793A>C
ENST00000382103.6:c.995A>C	ENSP00000371535.2:p.Asn332Thr
ENST00000503150.1:c.277A>C
ENST00000505513.1:n.295A>C
ENST00000514585.5:c.*696A>C	ENSP00000421880.1:n.*696A>C
NM_016955.3:c.995A>C	NP_058651.3:p.Asn332Thr
XM_005248168.2:c.758A>C	XP_005248225.1:p.Asn253Thr
XM_006713965.2:c.815A>C	XP_006714028.1:p.Asn272Thr
XM_011513846.1:c.992A>C	XP_011512148.1:p.Asn331Thr
XM_011513847.1:c.962A>C	XP_011512149.1:p.Asn321Thr
XM_011513848.1:c.815A>C	XP_011512150.1:p.Asn272Thr
XM_011513846.2:c.992A>C	XP_011512148.1:p.Asn331Thr
XM_011513847.2:c.962A>C	XP_011512149.1:p.Asn321Thr
XM_017008277.1:c.1250A>C	XP_016863766.1:p.Asn417Thr
XM_017008278.1:c.572A>C	XP_016863767.1:p.Asn191Thr
NM_016955.4:c.995A>C MANE Select	NP_058651.3:p.Asn332Thr