Canonical Allele Identifier: CA438732313

Gene: SEPSECS

Linked Data

• MyVariant Identifiers: chr4:g.25146453A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25144831A>C , CM000666.2:g.25144831A>C	GRCh38
NC_000004.11:g.25146453A>C , CM000666.1:g.25146453A>C	GRCh37
NC_000004.10:g.24755551A>C	NCBI36
NG_028222.1:g.20752T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.969T>G MANE Select	ENSP00000371535.2:p.Leu323=
ENST00000680581.1:c.969T>G	ENSP00000506483.1:p.Leu323=
ENST00000680824.1:n.2185T>G
ENST00000681071.1:n.1261T>G
ENST00000681341.1:n.2110T>G
ENST00000681948.1:c.1224T>G	ENSP00000505991.1:p.Leu408=
ENST00000358971.7:c.*767T>G	ENSP00000351857.3:n.*767T>G
ENST00000382103.6:c.969T>G	ENSP00000371535.2:p.Leu323=
ENST00000503150.1:c.251T>G
ENST00000505513.1:n.269T>G
ENST00000514585.5:c.*670T>G	ENSP00000421880.1:n.*670T>G
NM_016955.3:c.969T>G	NP_058651.3:p.Leu323=
XM_005248168.2:c.732T>G	XP_005248225.1:p.Leu244=
XM_006713965.2:c.789T>G	XP_006714028.1:p.Leu263=
XM_011513846.1:c.966T>G	XP_011512148.1:p.Leu322=
XM_011513847.1:c.936T>G	XP_011512149.1:p.Leu312=
XM_011513848.1:c.789T>G	XP_011512150.1:p.Leu263=
XM_011513846.2:c.966T>G	XP_011512148.1:p.Leu322=
XM_011513847.2:c.936T>G	XP_011512149.1:p.Leu312=
XM_017008277.1:c.1224T>G	XP_016863766.1:p.Leu408=
XM_017008278.1:c.546T>G	XP_016863767.1:p.Leu182=
NM_016955.4:c.969T>G MANE Select	NP_058651.3:p.Leu323=