Canonical Allele Identifier: CA1060322918

Gene: SEPSECS

Linked Data

• gnomAD v3: 4-25144305-A-C
• gnomAD v4: 4-25144305-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25144305A>C , CM000666.2:g.25144305A>C	GRCh38
NC_000004.11:g.25145927A>C , CM000666.1:g.25145927A>C	GRCh37
NC_000004.10:g.24755025A>C	NCBI36
NG_028222.1:g.21278T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.1026+469T>G MANE Select	ENSP00000371535.2:n.1026+469T>G
ENST00000680581.1:c.1026+469T>G	ENSP00000506483.1:n.1026+469T>G
ENST00000680824.1:n.2242+469T>G
ENST00000681071.1:n.1318+469T>G
ENST00000681341.1:n.2167+469T>G
ENST00000681948.1:c.1281+469T>G	ENSP00000505991.1:n.1281+469T>G
ENST00000358971.7:c.*824+469T>G	ENSP00000351857.3:n.*824+469T>G
ENST00000382103.6:c.1026+469T>G	ENSP00000371535.2:n.1026+469T>G
ENST00000503150.1:c.308+469T>G
ENST00000505513.1:n.326+469T>G
ENST00000514585.5:c.*727+469T>G	ENSP00000421880.1:n.*727+469T>G
NM_016955.3:c.1026+469T>G	NP_058651.3:n.1026+469T>G
XM_005248168.2:c.789+469T>G	XP_005248225.1:n.789+469T>G
XM_006713965.2:c.846+469T>G	XP_006714028.1:n.846+469T>G
XM_011513846.1:c.1023+469T>G	XP_011512148.1:n.1023+469T>G
XM_011513847.1:c.993+469T>G	XP_011512149.1:n.993+469T>G
XM_011513848.1:c.846+469T>G	XP_011512150.1:n.846+469T>G
XM_011513846.2:c.1023+469T>G	XP_011512148.1:n.1023+469T>G
XM_011513847.2:c.993+469T>G	XP_011512149.1:n.993+469T>G
XM_017008277.1:c.1281+469T>G	XP_016863766.1:n.1281+469T>G
XM_017008278.1:c.603+469T>G	XP_016863767.1:n.603+469T>G
NM_016955.4:c.1026+469T>G MANE Select	NP_058651.3:n.1026+469T>G