Canonical Allele Identifier: CA518836009

Gene: IGSF1

Linked Data

• MyVariant Identifiers: chrX:g.130411837G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.131277863G>A , CM000685.2:g.131277863G>A	GRCh38
NC_000023.10:g.130411837G>A , CM000685.1:g.130411837G>A	GRCh37
NC_000023.9:g.130239518G>A	NCBI36
NG_021190.2:g.126841C>T
NG_021190.3:g.306037C>T
NG_021190.4:g.306037C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361420.8:c.2313C>T MANE Select	ENSP00000355010.3:p.Val771=
ENST00000370903.8:c.2328C>T	ENSP00000359940.3:p.Val776=
ENST00000651402.1:c.10-2986C>T
ENST00000651526.1:n.715C>T
ENST00000651556.1:c.2313C>T	ENSP00000498789.1:p.Val771=
ENST00000652189.1:c.2313C>T	ENSP00000498607.1:p.Val771=
ENST00000361420.7:c.2313C>T	ENSP00000355010.3:p.Val771=
ENST00000370903.7:c.2328C>T	ENSP00000359940.3:p.Val776=
ENST00000370904.6:c.2286C>T	ENSP00000359941.1:p.Val762=
ENST00000370910.5:c.2286C>T	ENSP00000359947.1:p.Val762=
NM_001170961.1:c.2328C>T	NP_001164432.1:p.Val776=
NM_001170962.1:c.2286C>T	NP_001164433.1:p.Val762=
NM_001555.4:c.2313C>T	NP_001546.2:p.Val771=
XM_011531330.1:c.2328C>T	XP_011529632.1:p.Val776=
XM_011531331.1:c.2328C>T	XP_011529633.1:p.Val776=
XM_011531332.1:c.2328C>T	XP_011529634.1:p.Val776=
XM_011531333.1:c.2328C>T	XP_011529635.1:p.Val776=
XM_011531334.1:c.2328C>T	XP_011529636.1:p.Val776=
XM_011531335.1:c.555C>T	XP_011529637.1:p.Val185=
XM_011531333.2:c.2328C>T	XP_011529635.1:p.Val776=
XM_011531334.2:c.2328C>T	XP_011529636.1:p.Val776=
NM_001555.5:c.2313C>T MANE Select	NP_001546.2:p.Val771=
NM_001170962.2:c.2286C>T	NP_001164433.1:p.Val762=
NM_001170961.2:c.2328C>T	NP_001164432.1:p.Val776=