Canonical Allele Identifier: CA730035395

Gene: INAVA

Linked Data

• dbSNP Id: rs1171994515
• MyVariant Identifiers: chr1:g.200881691G>A (hg19) ; chr1:g.200912563G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.200912563G>A , CM000663.2:g.200912563G>A	GRCh38
NC_000001.10:g.200881691G>A , CM000663.1:g.200881691G>A	GRCh37
NC_000001.9:g.199148314G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000413687.3:c.1644+426G>A MANE Select	ENSP00000392105.2:n.1644+426G>A
ENST00000367342.8:c.1899+426G>A	ENSP00000356311.4:n.1899+426G>A
ENST00000413687.2:c.1644+426G>A	ENSP00000392105.2:n.1644+426G>A
ENST00000465162.1:n.179+426G>A
NM_001142569.2:c.1644+426G>A	NP_001136041.1:n.1644+426G>A
NM_018265.3:c.1941+426G>A	NP_060735.3:n.1941+426G>A
XM_011509754.1:c.1644+426G>A	XP_011508056.1:n.1644+426G>A
XM_011509755.1:c.1644+426G>A	XP_011508057.1:n.1644+426G>A
XM_011509754.2:c.1644+426G>A	XP_011508056.1:n.1644+426G>A
NM_001142569.3:c.1644+426G>A MANE Select	NP_001136041.1:n.1644+426G>A
NM_001367289.1:c.1584+486G>A	NP_001354218.1:n.1584+486G>A
NM_001367290.1:c.1107+426G>A	NP_001354219.1:n.1107+426G>A
NM_018265.4:c.1899+426G>A	NP_060735.4:n.1899+426G>A