Canonical Allele Identifier: CA93575917

Gene: SEPSECS

Linked Data

• dbSNP Id: rs925879303
• gnomAD v2: 4-25146281-G-A
• gnomAD v3: 4-25144659-G-A
• gnomAD v4: 4-25144659-G-A
• MyVariant Identifiers: chr4:g.25146281G>A (hg19) ; chr4:g.25144659G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25144659G>A , CM000666.2:g.25144659G>A	GRCh38
NC_000004.11:g.25146281G>A , CM000666.1:g.25146281G>A	GRCh37
NC_000004.10:g.24755379G>A	NCBI36
NG_028222.1:g.20924C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000382103.7:c.1026+115C>T MANE Select	ENSP00000371535.2:n.1026+115C>T
ENST00000680581.1:c.1026+115C>T	ENSP00000506483.1:n.1026+115C>T
ENST00000680824.1:n.2242+115C>T
ENST00000681071.1:n.1318+115C>T
ENST00000681341.1:n.2167+115C>T
ENST00000681948.1:c.1281+115C>T	ENSP00000505991.1:n.1281+115C>T
ENST00000358971.7:c.*824+115C>T	ENSP00000351857.3:n.*824+115C>T
ENST00000382103.6:c.1026+115C>T	ENSP00000371535.2:n.1026+115C>T
ENST00000503150.1:c.308+115C>T
ENST00000505513.1:n.326+115C>T
ENST00000514585.5:c.*727+115C>T	ENSP00000421880.1:n.*727+115C>T
NM_016955.3:c.1026+115C>T	NP_058651.3:n.1026+115C>T
XM_005248168.2:c.789+115C>T	XP_005248225.1:n.789+115C>T
XM_006713965.2:c.846+115C>T	XP_006714028.1:n.846+115C>T
XM_011513846.1:c.1023+115C>T	XP_011512148.1:n.1023+115C>T
XM_011513847.1:c.993+115C>T	XP_011512149.1:n.993+115C>T
XM_011513848.1:c.846+115C>T	XP_011512150.1:n.846+115C>T
XM_011513846.2:c.1023+115C>T	XP_011512148.1:n.1023+115C>T
XM_011513847.2:c.993+115C>T	XP_011512149.1:n.993+115C>T
XM_017008277.1:c.1281+115C>T	XP_016863766.1:n.1281+115C>T
XM_017008278.1:c.603+115C>T	XP_016863767.1:n.603+115C>T
NM_016955.4:c.1026+115C>T MANE Select	NP_058651.3:n.1026+115C>T