Canonical Allele Identifier: CA730035371

Gene: INAVA

Linked Data

• dbSNP Id: rs1322117882
• MyVariant Identifiers: chr1:g.200881554_200881556del (hg19) ; chr1:g.200912426_200912428del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.200912432_200912434del , CM000663.2:g.200912432_200912434del	GRCh38
NC_000001.10:g.200881560_200881562del , CM000663.1:g.200881560_200881562del	GRCh37
NC_000001.9:g.199148183_199148185del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000413687.3:c.1644+295_1644+297del MANE Select	ENSP00000392105.2:n.1644+295_1644+297del
ENST00000367342.8:c.1899+295_1899+297del	ENSP00000356311.4:n.1899+295_1899+297del
ENST00000413687.2:c.1644+295_1644+297del	ENSP00000392105.2:n.1644+295_1644+297del
ENST00000465162.1:n.179+295_179+297del
NM_001142569.2:c.1644+295_1644+297del	NP_001136041.1:n.1644+295_1644+297del
NM_018265.3:c.1941+295_1941+297del	NP_060735.3:n.1941+295_1941+297del
XM_011509754.1:c.1644+295_1644+297del	XP_011508056.1:n.1644+295_1644+297del
XM_011509755.1:c.1644+295_1644+297del	XP_011508057.1:n.1644+295_1644+297del
XM_011509754.2:c.1644+295_1644+297del	XP_011508056.1:n.1644+295_1644+297del
NM_001142569.3:c.1644+295_1644+297del MANE Select	NP_001136041.1:n.1644+295_1644+297del
NM_001367289.1:c.1584+355_1584+357del	NP_001354218.1:n.1584+355_1584+357del
NM_001367290.1:c.1107+295_1107+297del	NP_001354219.1:n.1107+295_1107+297del
NM_018265.4:c.1899+295_1899+297del	NP_060735.4:n.1899+295_1899+297del