Canonical Allele Identifier: CA618703952

Gene: ITGA11

Linked Data

• dbSNP Id: rs1383552196
• gnomAD v2: 15-68628207-ATCTT-A
• gnomAD v3: 15-68335869-ATCTT-A
• gnomAD v4: 15-68335869-ATCTT-A
• MyVariant Identifiers: chr15:g.68628208_68628211del (hg19) ; chr15:g.68335870_68335873del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68335871_68335874del , CM000677.2:g.68335871_68335874del	GRCh38
NC_000015.9:g.68628209_68628212del , CM000677.1:g.68628209_68628212del	GRCh37
NC_000015.8:g.66415263_66415266del	NCBI36
NG_046911.1:g.101288_101291del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315757.9:c.1277-28_1277-25del MANE Select	ENSP00000327290.7:n.1277-28_1277-25del
ENST00000315757.8:c.1277-28_1277-25del	ENSP00000327290.7:n.1277-28_1277-25del
ENST00000423218.6:c.1277-28_1277-25del	ENSP00000403392.2:n.1277-28_1277-25del
ENST00000566429.1:n.197-59_197-56del
ENST00000569346.5:n.228_231del
NM_001004439.1:c.1277-28_1277-25del	NP_001004439.1:n.1277-28_1277-25del
XM_005254228.2:c.971-28_971-25del	XP_005254285.1:n.971-28_971-25del
XM_011521363.1:c.1070-28_1070-25del	XP_011519665.1:n.1070-28_1070-25del
XM_005254228.3:c.971-28_971-25del	XP_005254285.1:n.971-28_971-25del
XM_011521363.2:c.1070-28_1070-25del	XP_011519665.1:n.1070-28_1070-25del
NM_001004439.2:c.1277-28_1277-25del MANE Select	NP_001004439.1:n.1277-28_1277-25del