Canonical Allele Identifier: CA2670381

Gene: IGSF10

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.151447744G>C , CM000665.2:g.151447744G>C	GRCh38
NC_000003.11:g.151165532G>C , CM000665.1:g.151165532G>C	GRCh37
NC_000003.10:g.152648222G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_178822.5:c.2237C>G MANE Select	NP_849144.2:p.Pro746Arg
ENST00000282466.4:c.2237C>G MANE Select	ENSP00000282466.3:p.Pro746Arg
NM_001385060.1:c.2237C>G	NP_001371989.1:p.Pro746Arg
NM_001385061.1:c.2237C>G	NP_001371990.1:p.Pro746Arg
NM_001385062.1:c.2237C>G	NP_001371991.1:p.Pro746Arg
NM_001385063.1:c.2237C>G	NP_001371992.1:p.Pro746Arg
NM_178822.4:c.2237C>G	NP_849144.2:p.Pro746Arg
ENST00000282466.3:c.2237C>G	ENSP00000282466.3:p.Pro746Arg
XM_011512708.1:c.2453C>G	XP_011511010.1:p.Pro818Arg
XM_011512708.2:c.2453C>G	XP_011511010.1:p.Pro818Arg
XM_011512709.1:c.2237C>G	XP_011511011.1:p.Pro746Arg
XM_011512709.2:c.2237C>G	XP_011511011.1:p.Pro746Arg