Canonical Allele Identifier: CA272443242

Gene: ITGA11

Linked Data

• dbSNP Id: rs544141300
• gnomAD v3: 15-68335626-T-C
• gnomAD v4: 15-68335626-T-C
• MyVariant Identifiers: chr15:g.68627964T>C (hg19) ; chr15:g.68335626T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68335626T>C , CM000677.2:g.68335626T>C	GRCh38
NC_000015.9:g.68627964T>C , CM000677.1:g.68627964T>C	GRCh37
NC_000015.8:g.66415018T>C	NCBI36
NG_046911.1:g.101535A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315757.9:c.1425+71A>G MANE Select	ENSP00000327290.7:n.1425+71A>G
ENST00000315757.8:c.1425+71A>G	ENSP00000327290.7:n.1425+71A>G
ENST00000423218.6:c.1425+71A>G	ENSP00000403392.2:n.1425+71A>G
ENST00000566429.1:n.314+71A>G
ENST00000569346.5:n.404+71A>G
NM_001004439.1:c.1425+71A>G	NP_001004439.1:n.1425+71A>G
XM_005254228.2:c.1119+71A>G	XP_005254285.1:n.1119+71A>G
XM_011521363.1:c.1218+71A>G	XP_011519665.1:n.1218+71A>G
XM_005254228.3:c.1119+71A>G	XP_005254285.1:n.1119+71A>G
XM_011521363.2:c.1218+71A>G	XP_011519665.1:n.1218+71A>G
NM_001004439.2:c.1425+71A>G MANE Select	NP_001004439.1:n.1425+71A>G