Canonical Allele Identifier: CA7631840

Gene: ITGA11

Linked Data

• dbSNP Id: rs754736026
• ExAC: 15:68628023 C / T
• gnomAD v4: 15-68335685-C-T
• MyVariant Identifiers: chr15:g.68628023C>T (hg19) ; chr15:g.68335685C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68335685C>T , CM000677.2:g.68335685C>T	GRCh38
NC_000015.9:g.68628023C>T , CM000677.1:g.68628023C>T	GRCh37
NC_000015.8:g.66415077C>T	NCBI36
NG_046911.1:g.101476G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315757.9:c.1425+12G>A MANE Select	ENSP00000327290.7:n.1425+12G>A
ENST00000315757.8:c.1425+12G>A	ENSP00000327290.7:n.1425+12G>A
ENST00000423218.6:c.1425+12G>A	ENSP00000403392.2:n.1425+12G>A
ENST00000566429.1:n.314+12G>A
ENST00000569346.5:n.404+12G>A
NM_001004439.1:c.1425+12G>A	NP_001004439.1:n.1425+12G>A
XM_005254228.2:c.1119+12G>A	XP_005254285.1:n.1119+12G>A
XM_011521363.1:c.1218+12G>A	XP_011519665.1:n.1218+12G>A
XM_005254228.3:c.1119+12G>A	XP_005254285.1:n.1119+12G>A
XM_011521363.2:c.1218+12G>A	XP_011519665.1:n.1218+12G>A
NM_001004439.2:c.1425+12G>A MANE Select	NP_001004439.1:n.1425+12G>A