Canonical Allele Identifier: CA438732325

Gene: SEPSECS

Linked Data

• MyVariant Identifiers: chr4:g.25146468A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25144846A>G , CM000666.2:g.25144846A>G	GRCh38
NC_000004.11:g.25146468A>G , CM000666.1:g.25146468A>G	GRCh37
NC_000004.10:g.24755566A>G	NCBI36
NG_028222.1:g.20737T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.954T>C MANE Select	ENSP00000371535.2:p.Pro318=
ENST00000680581.1:c.954T>C	ENSP00000506483.1:p.Pro318=
ENST00000680824.1:n.2170T>C
ENST00000681071.1:n.1246T>C
ENST00000681341.1:n.2095T>C
ENST00000681948.1:c.1209T>C	ENSP00000505991.1:p.Pro403=
ENST00000358971.7:c.*752T>C	ENSP00000351857.3:n.*752T>C
ENST00000382103.6:c.954T>C	ENSP00000371535.2:p.Pro318=
ENST00000503150.1:c.236T>C
ENST00000505513.1:n.254T>C
ENST00000514585.5:c.*655T>C	ENSP00000421880.1:n.*655T>C
NM_016955.3:c.954T>C	NP_058651.3:p.Pro318=
XM_005248168.2:c.717T>C	XP_005248225.1:p.Pro239=
XM_006713965.2:c.774T>C	XP_006714028.1:p.Pro258=
XM_011513846.1:c.951T>C	XP_011512148.1:p.Pro317=
XM_011513847.1:c.921T>C	XP_011512149.1:p.Pro307=
XM_011513848.1:c.774T>C	XP_011512150.1:p.Pro258=
XM_011513846.2:c.951T>C	XP_011512148.1:p.Pro317=
XM_011513847.2:c.921T>C	XP_011512149.1:p.Pro307=
XM_017008277.1:c.1209T>C	XP_016863766.1:p.Pro403=
XM_017008278.1:c.531T>C	XP_016863767.1:p.Pro177=
NM_016955.4:c.954T>C MANE Select	NP_058651.3:p.Pro318=