Canonical Allele Identifier: CA93575739

Gene: SEPSECS

Linked Data

• dbSNP Id: rs978625398
• MyVariant Identifiers: chr4:g.25145967_25145971del (hg19) ; chr4:g.25144345_25144349del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25144346_25144350del , CM000666.2:g.25144346_25144350del	GRCh38
NC_000004.11:g.25145968_25145972del , CM000666.1:g.25145968_25145972del	GRCh37
NC_000004.10:g.24755066_24755070del	NCBI36
NG_028222.1:g.21234_21238del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.1026+425_1026+429del MANE Select	ENSP00000371535.2:n.1026+425_1026+429del
ENST00000680581.1:c.1026+425_1026+429del	ENSP00000506483.1:n.1026+425_1026+429del
ENST00000680824.1:n.2242+425_2242+429del
ENST00000681071.1:n.1318+425_1318+429del
ENST00000681341.1:n.2167+425_2167+429del
ENST00000681948.1:c.1281+425_1281+429del	ENSP00000505991.1:n.1281+425_1281+429del
ENST00000358971.7:c.*824+425_*824+429del	ENSP00000351857.3:n.*824+425_*824+429del
ENST00000382103.6:c.1026+425_1026+429del	ENSP00000371535.2:n.1026+425_1026+429del
ENST00000503150.1:c.308+425_308+429del
ENST00000505513.1:n.326+425_326+429del
ENST00000514585.5:c.*727+425_*727+429del	ENSP00000421880.1:n.*727+425_*727+429del
NM_016955.3:c.1026+425_1026+429del	NP_058651.3:n.1026+425_1026+429del
XM_005248168.2:c.789+425_789+429del	XP_005248225.1:n.789+425_789+429del
XM_006713965.2:c.846+425_846+429del	XP_006714028.1:n.846+425_846+429del
XM_011513846.1:c.1023+425_1023+429del	XP_011512148.1:n.1023+425_1023+429del
XM_011513847.1:c.993+425_993+429del	XP_011512149.1:n.993+425_993+429del
XM_011513848.1:c.846+425_846+429del	XP_011512150.1:n.846+425_846+429del
XM_011513846.2:c.1023+425_1023+429del	XP_011512148.1:n.1023+425_1023+429del
XM_011513847.2:c.993+425_993+429del	XP_011512149.1:n.993+425_993+429del
XM_017008277.1:c.1281+425_1281+429del	XP_016863766.1:n.1281+425_1281+429del
XM_017008278.1:c.603+425_603+429del	XP_016863767.1:n.603+425_603+429del
NM_016955.4:c.1026+425_1026+429del MANE Select	NP_058651.3:n.1026+425_1026+429del