Canonical Allele Identifier: CA7631859

Gene: ITGA11

Linked Data

• dbSNP Id: rs747868028
• ExAC: 15:68628121 G / A
• gnomAD v2: 15-68628121-G-A
• gnomAD v3: 15-68335783-G-A
• gnomAD v4: 15-68335783-G-A
• MyVariant Identifiers: chr15:g.68628121G>A (hg19) ; chr15:g.68335783G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68335783G>A , CM000677.2:g.68335783G>A	GRCh38
NC_000015.9:g.68628121G>A , CM000677.1:g.68628121G>A	GRCh37
NC_000015.8:g.66415175G>A	NCBI36
NG_046911.1:g.101378C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315757.9:c.1339C>T MANE Select	ENSP00000327290.7:p.Arg447Trp
ENST00000315757.8:c.1339C>T	ENSP00000327290.7:p.Arg447Trp
ENST00000423218.6:c.1339C>T	ENSP00000403392.2:p.Arg447Trp
ENST00000566429.1:n.228C>T
ENST00000569346.5:n.318C>T
NM_001004439.1:c.1339C>T	NP_001004439.1:p.Arg447Trp
XM_005254228.2:c.1033C>T	XP_005254285.1:p.Arg345Trp
XM_011521363.1:c.1132C>T	XP_011519665.1:p.Arg378Trp
XM_005254228.3:c.1033C>T	XP_005254285.1:p.Arg345Trp
XM_011521363.2:c.1132C>T	XP_011519665.1:p.Arg378Trp
NM_001004439.2:c.1339C>T MANE Select	NP_001004439.1:p.Arg447Trp