Canonical Allele Identifier: CA356542845

Gene: SEPSECS

Linked Data

• gnomAD v4: 4-25156958-C-A
• MyVariant Identifiers: chr4:g.25158580C>A (hg19) ; chr4:g.25156958C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25156958C>A , CM000666.2:g.25156958C>A	GRCh38
NC_000004.11:g.25158580C>A , CM000666.1:g.25158580C>A	GRCh37
NC_000004.10:g.24767678C>A	NCBI36
NG_028222.1:g.8625G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.286G>T MANE Select	ENSP00000371535.2:p.Gly96Ter
ENST00000680581.1:c.286G>T	ENSP00000506483.1:p.Gly96Ter
ENST00000680824.1:n.1502G>T
ENST00000681071.1:n.578G>T
ENST00000681166.1:n.1333G>T
ENST00000681341.1:n.1427G>T
ENST00000681640.1:n.380G>T
ENST00000681948.1:c.541G>T	ENSP00000505991.1:p.Gly181Ter
ENST00000358971.7:c.*84G>T	ENSP00000351857.3:n.*84G>T
ENST00000382103.6:c.286G>T	ENSP00000371535.2:p.Gly96Ter
ENST00000514585.5:c.131G>T	ENSP00000421880.1:p.Trp44Leu
NM_016955.3:c.286G>T	NP_058651.3:p.Gly96Ter
XM_005248168.2:c.49G>T	XP_005248225.1:p.Gly17Ter
XM_006713965.2:c.106G>T	XP_006714028.1:p.Gly36Ter
XM_011513846.1:c.283G>T	XP_011512148.1:p.Gly95Ter
XM_011513847.1:c.253G>T	XP_011512149.1:p.Gly85Ter
XM_011513848.1:c.106G>T	XP_011512150.1:p.Gly36Ter
XM_011513846.2:c.283G>T	XP_011512148.1:p.Gly95Ter
XM_011513847.2:c.253G>T	XP_011512149.1:p.Gly85Ter
XM_017008277.1:c.541G>T	XP_016863766.1:p.Gly181Ter
XM_017008278.1:c.-138G>T	XP_016863767.1:n.-138G>T
NM_016955.4:c.286G>T MANE Select	NP_058651.3:p.Gly96Ter