Canonical Allele Identifier: CA2558460006

Gene: INAVA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.200912379T>G , CM000663.2:g.200912379T>G	GRCh38
NC_000001.10:g.200881507T>G , CM000663.1:g.200881507T>G	GRCh37
NC_000001.9:g.199148130T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000413687.3:c.1644+242T>G MANE Select	ENSP00000392105.2:n.1644+242T>G
ENST00000367342.8:c.1899+242T>G	ENSP00000356311.4:n.1899+242T>G
ENST00000413687.2:c.1644+242T>G	ENSP00000392105.2:n.1644+242T>G
ENST00000465162.1:n.179+242T>G
NM_001142569.2:c.1644+242T>G	NP_001136041.1:n.1644+242T>G
NM_018265.3:c.1941+242T>G	NP_060735.3:n.1941+242T>G
XM_011509754.1:c.1644+242T>G	XP_011508056.1:n.1644+242T>G
XM_011509755.1:c.1644+242T>G	XP_011508057.1:n.1644+242T>G
XM_011509754.2:c.1644+242T>G	XP_011508056.1:n.1644+242T>G
NM_001142569.3:c.1644+242T>G MANE Select	NP_001136041.1:n.1644+242T>G
NM_001367289.1:c.1584+302T>G	NP_001354218.1:n.1584+302T>G
NM_001367290.1:c.1107+242T>G	NP_001354219.1:n.1107+242T>G
NM_018265.4:c.1899+242T>G	NP_060735.4:n.1899+242T>G