Canonical Allele Identifier: CA7631853

Gene: ITGA11

Linked Data

• dbSNP Id: rs750558014
• ExAC: 15:68628100 C / A
• gnomAD v2: 15-68628100-C-A
• gnomAD v3: 15-68335762-C-A
• gnomAD v4: 15-68335762-C-A
• MyVariant Identifiers: chr15:g.68628100C>A (hg19) ; chr15:g.68335762C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68335762C>A , CM000677.2:g.68335762C>A	GRCh38
NC_000015.9:g.68628100C>A , CM000677.1:g.68628100C>A	GRCh37
NC_000015.8:g.66415154C>A	NCBI36
NG_046911.1:g.101399G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315757.9:c.1360G>T MANE Select	ENSP00000327290.7:p.Val454Phe
ENST00000315757.8:c.1360G>T	ENSP00000327290.7:p.Val454Phe
ENST00000423218.6:c.1360G>T	ENSP00000403392.2:p.Val454Phe
ENST00000566429.1:n.249G>T
ENST00000569346.5:n.339G>T
NM_001004439.1:c.1360G>T	NP_001004439.1:p.Val454Phe
XM_005254228.2:c.1054G>T	XP_005254285.1:p.Val352Phe
XM_011521363.1:c.1153G>T	XP_011519665.1:p.Val385Phe
XM_005254228.3:c.1054G>T	XP_005254285.1:p.Val352Phe
XM_011521363.2:c.1153G>T	XP_011519665.1:p.Val385Phe
NM_001004439.2:c.1360G>T MANE Select	NP_001004439.1:p.Val454Phe