Canonical Allele Identifier: CA618703955

Gene: ITGA11

Linked Data

• dbSNP Id: rs1156917951
• gnomAD v2: 15-68628211-T-G
• gnomAD v4: 15-68335873-T-G
• MyVariant Identifiers: chr15:g.68628211T>G (hg19) ; chr15:g.68335873T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68335873T>G , CM000677.2:g.68335873T>G	GRCh38
NC_000015.9:g.68628211T>G , CM000677.1:g.68628211T>G	GRCh37
NC_000015.8:g.66415265T>G	NCBI36
NG_046911.1:g.101288A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315757.9:c.1277-28A>C MANE Select	ENSP00000327290.7:n.1277-28A>C
ENST00000315757.8:c.1277-28A>C	ENSP00000327290.7:n.1277-28A>C
ENST00000423218.6:c.1277-28A>C	ENSP00000403392.2:n.1277-28A>C
ENST00000566429.1:n.197-59A>C
ENST00000569346.5:n.228A>C
NM_001004439.1:c.1277-28A>C	NP_001004439.1:n.1277-28A>C
XM_005254228.2:c.971-28A>C	XP_005254285.1:n.971-28A>C
XM_011521363.1:c.1070-28A>C	XP_011519665.1:n.1070-28A>C
XM_005254228.3:c.971-28A>C	XP_005254285.1:n.971-28A>C
XM_011521363.2:c.1070-28A>C	XP_011519665.1:n.1070-28A>C
NM_001004439.2:c.1277-28A>C MANE Select	NP_001004439.1:n.1277-28A>C