Canonical Allele Identifier: CA93584621

Gene: SEPSECS

Linked Data

• dbSNP Id: rs962402637
• gnomAD v2: 4-25158027-A-T
• gnomAD v3: 4-25156405-A-T
• gnomAD v4: 4-25156405-A-T
• MyVariant Identifiers: chr4:g.25158027A>T (hg19) ; chr4:g.25156405A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25156405A>T , CM000666.2:g.25156405A>T	GRCh38
NC_000004.11:g.25158027A>T , CM000666.1:g.25158027A>T	GRCh37
NC_000004.10:g.24767125A>T	NCBI36
NG_028222.1:g.9178T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.389-210T>A MANE Select	ENSP00000371535.2:n.389-210T>A
ENST00000680581.1:c.389-210T>A	ENSP00000506483.1:n.389-210T>A
ENST00000680824.1:n.1605-210T>A
ENST00000681071.1:n.681-210T>A
ENST00000681166.1:n.1436-210T>A
ENST00000681341.1:n.1530-210T>A
ENST00000681640.1:n.483-210T>A
ENST00000681948.1:c.644-210T>A	ENSP00000505991.1:n.644-210T>A
ENST00000358971.7:c.*187-210T>A	ENSP00000351857.3:n.*187-210T>A
ENST00000382103.6:c.389-210T>A	ENSP00000371535.2:n.389-210T>A
ENST00000514585.5:c.*90-210T>A	ENSP00000421880.1:n.*90-210T>A
NM_016955.3:c.389-210T>A	NP_058651.3:n.389-210T>A
XM_005248168.2:c.152-210T>A	XP_005248225.1:n.152-210T>A
XM_006713965.2:c.209-210T>A	XP_006714028.1:n.209-210T>A
XM_011513846.1:c.386-210T>A	XP_011512148.1:n.386-210T>A
XM_011513847.1:c.356-210T>A	XP_011512149.1:n.356-210T>A
XM_011513848.1:c.209-210T>A	XP_011512150.1:n.209-210T>A
XM_011513846.2:c.386-210T>A	XP_011512148.1:n.386-210T>A
XM_011513847.2:c.356-210T>A	XP_011512149.1:n.356-210T>A
XM_017008277.1:c.644-210T>A	XP_016863766.1:n.644-210T>A
XM_017008278.1:c.-35-210T>A	XP_016863767.1:n.-35-210T>A
NM_016955.4:c.389-210T>A MANE Select	NP_058651.3:n.389-210T>A