Canonical Allele Identifier: CA1219517269

Gene: INAVA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.200912437_200912438delinsCA , CM000663.2:g.200912437_200912438delinsCA	GRCh38
NC_000001.10:g.200881565_200881566delinsCA , CM000663.1:g.200881565_200881566delinsCA	GRCh37
NC_000001.9:g.199148188_199148189delinsCA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000413687.3:c.1644+300_1644+301delinsCA MANE Select	ENSP00000392105.2:n.1644+300_1644+301delinsCA
ENST00000367342.8:c.1899+300_1899+301delinsCA	ENSP00000356311.4:n.1899+300_1899+301delinsCA
ENST00000413687.2:c.1644+300_1644+301delinsCA	ENSP00000392105.2:n.1644+300_1644+301delinsCA
ENST00000465162.1:n.179+300_179+301delinsCA
NM_001142569.2:c.1644+300_1644+301delinsCA	NP_001136041.1:n.1644+300_1644+301delinsCA
NM_018265.3:c.1941+300_1941+301delinsCA	NP_060735.3:n.1941+300_1941+301delinsCA
XM_011509754.1:c.1644+300_1644+301delinsCA	XP_011508056.1:n.1644+300_1644+301delinsCA
XM_011509755.1:c.1644+300_1644+301delinsCA	XP_011508057.1:n.1644+300_1644+301delinsCA
XM_011509754.2:c.1644+300_1644+301delinsCA	XP_011508056.1:n.1644+300_1644+301delinsCA
NM_001142569.3:c.1644+300_1644+301delinsCA MANE Select	NP_001136041.1:n.1644+300_1644+301delinsCA
NM_001367289.1:c.1584+360_1584+361delinsCA	NP_001354218.1:n.1584+360_1584+361delinsCA
NM_001367290.1:c.1107+300_1107+301delinsCA	NP_001354219.1:n.1107+300_1107+301delinsCA
NM_018265.4:c.1899+300_1899+301delinsCA	NP_060735.4:n.1899+300_1899+301delinsCA