Canonical Allele Identifier: CA2458672150
Gene: IGSF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.131277851T= , CM000685.2:g.131277851T= GRCh38
NC_000023.10:g.130411825T= , CM000685.1:g.130411825T= GRCh37
NC_000023.9:g.130239506T= NCBI36
NG_021190.2:g.126853A=
NG_021190.3:g.306049A=
NG_021190.4:g.306049A=

Transcript Alleles

HGVS Amino-acid change
ENST00000361420.8:c.2320+5A= MANE Select ENSP00000355010.3:n.2320+5A=
ENST00000370903.8:c.2335+5A= ENSP00000359940.3:n.2335+5A=
ENST00000651402.1:c.10-2974A=
ENST00000651526.1:n.722+5A=
ENST00000651556.1:c.2320+5A= ENSP00000498789.1:n.2320+5A=
ENST00000652189.1:c.2320+5A= ENSP00000498607.1:n.2320+5A=
ENST00000361420.7:c.2320+5A= ENSP00000355010.3:n.2320+5A=
ENST00000370903.7:c.2335+5A= ENSP00000359940.3:n.2335+5A=
ENST00000370904.6:c.2293+5A= ENSP00000359941.1:n.2293+5A=
ENST00000370910.5:c.2293+5A= ENSP00000359947.1:n.2293+5A=
NM_001170961.1:c.2335+5A= NP_001164432.1:n.2335+5A=
NM_001170962.1:c.2293+5A= NP_001164433.1:n.2293+5A=
NM_001555.4:c.2320+5A= NP_001546.2:n.2320+5A=
XM_011531330.1:c.2335+5A= XP_011529632.1:n.2335+5A=
XM_011531331.1:c.2335+5A= XP_011529633.1:n.2335+5A=
XM_011531332.1:c.2335+5A= XP_011529634.1:n.2335+5A=
XM_011531333.1:c.2335+5A= XP_011529635.1:n.2335+5A=
XM_011531334.1:c.2335+5A= XP_011529636.1:n.2335+5A=
XM_011531335.1:c.562+5A= XP_011529637.1:n.562+5A=
XM_011531333.2:c.2335+5A= XP_011529635.1:n.2335+5A=
XM_011531334.2:c.2335+5A= XP_011529636.1:n.2335+5A=
NM_001555.5:c.2320+5A= MANE Select NP_001546.2:n.2320+5A=
NM_001170962.2:c.2293+5A= NP_001164433.1:n.2293+5A=
NM_001170961.2:c.2335+5A= NP_001164432.1:n.2335+5A=