Canonical Allele Identifier: CA15108711
Gene: INAVA HGNC NCBI

Linked Data

dbSNP Id: rs7554511
gnomAD v2: 1-200877562-C-A
gnomAD v3: 1-200908434-C-A
gnomAD v4: 1-200908434-C-A
MyVariant Identifiers: chr1:g.200877562C>A (hg19) chr1:g.200908434C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.200908434C>A , CM000663.2:g.200908434C>A GRCh38
NC_000001.10:g.200877562C>A , CM000663.1:g.200877562C>A GRCh37
NC_000001.9:g.199144185C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000413687.3:c.575-296C>A MANE Select ENSP00000392105.2:n.575-296C>A
ENST00000367342.8:c.830-296C>A ENSP00000356311.4:n.830-296C>A
ENST00000413687.2:c.575-296C>A ENSP00000392105.2:n.575-296C>A
NM_001142569.2:c.575-296C>A NP_001136041.1:n.575-296C>A
NM_018265.3:c.872-296C>A NP_060735.3:n.872-296C>A
XM_011509754.1:c.575-296C>A XP_011508056.1:n.575-296C>A
XM_011509755.1:c.575-296C>A XP_011508057.1:n.575-296C>A
XM_011509756.1:c.649-296C>A XP_011508058.1:n.649-296C>A
XM_011509754.2:c.575-296C>A XP_011508056.1:n.575-296C>A
XM_011509756.2:c.649-296C>A XP_011508058.1:n.649-296C>A
NM_001142569.3:c.575-296C>A MANE Select NP_001136041.1:n.575-296C>A
NM_001367289.1:c.575-296C>A NP_001354218.1:n.575-296C>A
NM_001367290.1:c.40-298C>A NP_001354219.1:n.40-298C>A
NM_018265.4:c.830-296C>A NP_060735.4:n.830-296C>A
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