Canonical Allele Identifier: CA2669762

Gene: IGSF10

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.151443640T>C , CM000665.2:g.151443640T>C	GRCh38
NC_000003.11:g.151161428T>C , CM000665.1:g.151161428T>C	GRCh37
NC_000003.10:g.152644118T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_178822.5:c.5307A>G MANE Select	NP_849144.2:p.Ala1769=
ENST00000282466.4:c.5307A>G MANE Select	ENSP00000282466.3:p.Ala1769=
NM_001385060.1:c.5307A>G	NP_001371989.1:p.Ala1769=
NM_001385061.1:c.5307A>G	NP_001371990.1:p.Ala1769=
NM_001385062.1:c.5307A>G	NP_001371991.1:p.Ala1769=
NM_001385063.1:c.5307A>G	NP_001371992.1:p.Ala1769=
NM_178822.4:c.5307A>G	NP_849144.2:p.Ala1769=
ENST00000282466.3:c.5307A>G	ENSP00000282466.3:p.Ala1769=
XM_011512708.1:c.5523A>G	XP_011511010.1:p.Ala1841=
XM_011512708.2:c.5523A>G	XP_011511010.1:p.Ala1841=
XM_011512709.1:c.5307A>G	XP_011511011.1:p.Ala1769=
XM_011512709.2:c.5307A>G	XP_011511011.1:p.Ala1769=