Canonical Allele Identifier: CA7631867

Gene: ITGA11

Linked Data

• ClinVar Variation Id: 3111146
• ClinVar RCV Id: RCV004405526
• dbSNP Id: rs764516782
• ExAC: 15:68628145 G / A
• gnomAD v2: 15-68628145-G-A
• gnomAD v3: 15-68335807-G-A
• gnomAD v4: 15-68335807-G-A
• MyVariant Identifiers: chr15:g.68628145G>A (hg19) ; chr15:g.68335807G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68335807G>A , CM000677.2:g.68335807G>A	GRCh38
NC_000015.9:g.68628145G>A , CM000677.1:g.68628145G>A	GRCh37
NC_000015.8:g.66415199G>A	NCBI36
NG_046911.1:g.101354C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315757.9:c.1315C>T MANE Select	ENSP00000327290.7:p.Arg439Trp
ENST00000315757.8:c.1315C>T	ENSP00000327290.7:p.Arg439Trp
ENST00000423218.6:c.1315C>T	ENSP00000403392.2:p.Arg439Trp
ENST00000566429.1:n.204C>T
ENST00000569346.5:n.294C>T
NM_001004439.1:c.1315C>T	NP_001004439.1:p.Arg439Trp
XM_005254228.2:c.1009C>T	XP_005254285.1:p.Arg337Trp
XM_011521363.1:c.1108C>T	XP_011519665.1:p.Arg370Trp
XM_005254228.3:c.1009C>T	XP_005254285.1:p.Arg337Trp
XM_011521363.2:c.1108C>T	XP_011519665.1:p.Arg370Trp
NM_001004439.2:c.1315C>T MANE Select	NP_001004439.1:p.Arg439Trp