Canonical Allele Identifier: CA2694707897

Gene: IGSF1

Linked Data

• gnomAD v4: X-131277846-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.131277846T>A , CM000685.2:g.131277846T>A	GRCh38
NC_000023.10:g.130411820T>A , CM000685.1:g.130411820T>A	GRCh37
NC_000023.9:g.130239501T>A	NCBI36
NG_021190.2:g.126858A>T
NG_021190.3:g.306054A>T
NG_021190.4:g.306054A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000361420.8:c.2320+10A>T MANE Select	ENSP00000355010.3:n.2320+10A>T
ENST00000370903.8:c.2335+10A>T	ENSP00000359940.3:n.2335+10A>T
ENST00000651402.1:c.10-2969A>T
ENST00000651526.1:n.722+10A>T
ENST00000651556.1:c.2320+10A>T	ENSP00000498789.1:n.2320+10A>T
ENST00000652189.1:c.2320+10A>T	ENSP00000498607.1:n.2320+10A>T
ENST00000361420.7:c.2320+10A>T	ENSP00000355010.3:n.2320+10A>T
ENST00000370903.7:c.2335+10A>T	ENSP00000359940.3:n.2335+10A>T
ENST00000370904.6:c.2293+10A>T	ENSP00000359941.1:n.2293+10A>T
ENST00000370910.5:c.2293+10A>T	ENSP00000359947.1:n.2293+10A>T
NM_001170961.1:c.2335+10A>T	NP_001164432.1:n.2335+10A>T
NM_001170962.1:c.2293+10A>T	NP_001164433.1:n.2293+10A>T
NM_001555.4:c.2320+10A>T	NP_001546.2:n.2320+10A>T
XM_011531330.1:c.2335+10A>T	XP_011529632.1:n.2335+10A>T
XM_011531331.1:c.2335+10A>T	XP_011529633.1:n.2335+10A>T
XM_011531332.1:c.2335+10A>T	XP_011529634.1:n.2335+10A>T
XM_011531333.1:c.2335+10A>T	XP_011529635.1:n.2335+10A>T
XM_011531334.1:c.2335+10A>T	XP_011529636.1:n.2335+10A>T
XM_011531335.1:c.562+10A>T	XP_011529637.1:n.562+10A>T
XM_011531333.2:c.2335+10A>T	XP_011529635.1:n.2335+10A>T
XM_011531334.2:c.2335+10A>T	XP_011529636.1:n.2335+10A>T
NM_001555.5:c.2320+10A>T MANE Select	NP_001546.2:n.2320+10A>T
NM_001170962.2:c.2293+10A>T	NP_001164433.1:n.2293+10A>T
NM_001170961.2:c.2335+10A>T	NP_001164432.1:n.2335+10A>T