Canonical Allele Identifier: CA272443377

Gene: ITGA11

Linked Data

• dbSNP Id: rs559877389
• gnomAD v2: 15-68628252-T-C
• gnomAD v3: 15-68335914-T-C
• gnomAD v4: 15-68335914-T-C
• MyVariant Identifiers: chr15:g.68628252T>C (hg19) ; chr15:g.68335914T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68335914T>C , CM000677.2:g.68335914T>C	GRCh38
NC_000015.9:g.68628252T>C , CM000677.1:g.68628252T>C	GRCh37
NC_000015.8:g.66415306T>C	NCBI36
NG_046911.1:g.101247A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315757.9:c.1277-69A>G MANE Select	ENSP00000327290.7:n.1277-69A>G
ENST00000315757.8:c.1277-69A>G	ENSP00000327290.7:n.1277-69A>G
ENST00000423218.6:c.1277-69A>G	ENSP00000403392.2:n.1277-69A>G
ENST00000566429.1:n.197-100A>G
ENST00000569346.5:n.187A>G
NM_001004439.1:c.1277-69A>G	NP_001004439.1:n.1277-69A>G
XM_005254228.2:c.971-69A>G	XP_005254285.1:n.971-69A>G
XM_011521363.1:c.1070-69A>G	XP_011519665.1:n.1070-69A>G
XM_005254228.3:c.971-69A>G	XP_005254285.1:n.971-69A>G
XM_011521363.2:c.1070-69A>G	XP_011519665.1:n.1070-69A>G
NM_001004439.2:c.1277-69A>G MANE Select	NP_001004439.1:n.1277-69A>G