Canonical Allele Identifier: CA13237575

Gene: SEPHS1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.13321046A>T , CM000672.2:g.13321046A>T	GRCh38
NC_000010.10:g.13363046A>T , CM000672.1:g.13363046A>T	GRCh37
NC_000010.9:g.13403052A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327347.10:c.965-1690T>A MANE Select	ENSP00000367893.3:n.965-1690T>A
ENST00000327347.9:c.965-1690T>A	ENSP00000367893.3:n.965-1690T>A
ENST00000378614.8:c.752-1690T>A	ENSP00000367877.3:n.752-1690T>A
ENST00000545675.5:c.764-1690T>A	ENSP00000441119.2:n.764-1690T>A
NM_001195602.1:c.764-1690T>A	NP_001182531.1:n.764-1690T>A
NM_001195604.1:c.752-1690T>A	NP_001182533.1:n.752-1690T>A
NM_012247.4:c.965-1690T>A	NP_036379.2:n.965-1690T>A
XM_006717433.1:c.959-1690T>A	XP_006717496.1:n.959-1690T>A
XM_017015943.2:c.965-1690T>A	XP_016871432.1:n.965-1690T>A
XM_017015944.2:c.959-1690T>A	XP_016871433.1:n.959-1690T>A
XM_017015945.2:c.764-1690T>A	XP_016871434.1:n.764-1690T>A
NM_012247.5:c.965-1690T>A MANE Select	NP_036379.2:n.965-1690T>A
NM_001195604.2:c.752-1690T>A	NP_001182533.1:n.752-1690T>A
NM_001375769.1:c.959-1690T>A	NP_001362698.1:n.959-1690T>A
NR_164738.1:n.1555-1690T>A
NM_001195602.2:c.764-1690T>A	NP_001182531.1:n.764-1690T>A