Canonical Allele Identifier: CA392977860

Gene: ITGA11

Linked Data

• gnomAD v4: 15-68335794-G-T
• MyVariant Identifiers: chr15:g.68628132G>T (hg19) ; chr15:g.68335794G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68335794G>T , CM000677.2:g.68335794G>T	GRCh38
NC_000015.9:g.68628132G>T , CM000677.1:g.68628132G>T	GRCh37
NC_000015.8:g.66415186G>T	NCBI36
NG_046911.1:g.101367C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315757.9:c.1328C>A MANE Select	ENSP00000327290.7:p.Ala443Asp
ENST00000315757.8:c.1328C>A	ENSP00000327290.7:p.Ala443Asp
ENST00000423218.6:c.1328C>A	ENSP00000403392.2:p.Ala443Asp
ENST00000566429.1:n.217C>A
ENST00000569346.5:n.307C>A
NM_001004439.1:c.1328C>A	NP_001004439.1:p.Ala443Asp
XM_005254228.2:c.1022C>A	XP_005254285.1:p.Ala341Asp
XM_011521363.1:c.1121C>A	XP_011519665.1:p.Ala374Asp
XM_005254228.3:c.1022C>A	XP_005254285.1:p.Ala341Asp
XM_011521363.2:c.1121C>A	XP_011519665.1:p.Ala374Asp
NM_001004439.2:c.1328C>A MANE Select	NP_001004439.1:p.Ala443Asp