Canonical Allele Identifier: CA93575909

Gene: SEPSECS

Linked Data

• dbSNP Id: rs979110938
• gnomAD v2: 4-25146280-C-T
• gnomAD v3: 4-25144658-C-T
• gnomAD v4: 4-25144658-C-T
• MyVariant Identifiers: chr4:g.25146280C>T (hg19) ; chr4:g.25144658C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25144658C>T , CM000666.2:g.25144658C>T	GRCh38
NC_000004.11:g.25146280C>T , CM000666.1:g.25146280C>T	GRCh37
NC_000004.10:g.24755378C>T	NCBI36
NG_028222.1:g.20925G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000382103.7:c.1026+116G>A MANE Select	ENSP00000371535.2:n.1026+116G>A
ENST00000680581.1:c.1026+116G>A	ENSP00000506483.1:n.1026+116G>A
ENST00000680824.1:n.2242+116G>A
ENST00000681071.1:n.1318+116G>A
ENST00000681341.1:n.2167+116G>A
ENST00000681948.1:c.1281+116G>A	ENSP00000505991.1:n.1281+116G>A
ENST00000358971.7:c.*824+116G>A	ENSP00000351857.3:n.*824+116G>A
ENST00000382103.6:c.1026+116G>A	ENSP00000371535.2:n.1026+116G>A
ENST00000503150.1:c.308+116G>A
ENST00000505513.1:n.326+116G>A
ENST00000514585.5:c.*727+116G>A	ENSP00000421880.1:n.*727+116G>A
NM_016955.3:c.1026+116G>A	NP_058651.3:n.1026+116G>A
XM_005248168.2:c.789+116G>A	XP_005248225.1:n.789+116G>A
XM_006713965.2:c.846+116G>A	XP_006714028.1:n.846+116G>A
XM_011513846.1:c.1023+116G>A	XP_011512148.1:n.1023+116G>A
XM_011513847.1:c.993+116G>A	XP_011512149.1:n.993+116G>A
XM_011513848.1:c.846+116G>A	XP_011512150.1:n.846+116G>A
XM_011513846.2:c.1023+116G>A	XP_011512148.1:n.1023+116G>A
XM_011513847.2:c.993+116G>A	XP_011512149.1:n.993+116G>A
XM_017008277.1:c.1281+116G>A	XP_016863766.1:n.1281+116G>A
XM_017008278.1:c.603+116G>A	XP_016863767.1:n.603+116G>A
NM_016955.4:c.1026+116G>A MANE Select	NP_058651.3:n.1026+116G>A