Canonical Allele Identifier: CA7631874

Gene: ITGA11

Linked Data

• dbSNP Id: rs184820297
• ExAC: 15:68628194 A / G
• gnomAD v2: 15-68628194-A-G
• gnomAD v3: 15-68335856-A-G
• gnomAD v4: 15-68335856-A-G
• MyVariant Identifiers: chr15:g.68628194A>G (hg19) ; chr15:g.68335856A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68335856A>G , CM000677.2:g.68335856A>G	GRCh38
NC_000015.9:g.68628194A>G , CM000677.1:g.68628194A>G	GRCh37
NC_000015.8:g.66415248A>G	NCBI36
NG_046911.1:g.101305T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315757.9:c.1277-11T>C MANE Select	ENSP00000327290.7:n.1277-11T>C
ENST00000315757.8:c.1277-11T>C	ENSP00000327290.7:n.1277-11T>C
ENST00000423218.6:c.1277-11T>C	ENSP00000403392.2:n.1277-11T>C
ENST00000566429.1:n.197-42T>C
ENST00000569346.5:n.245T>C
NM_001004439.1:c.1277-11T>C	NP_001004439.1:n.1277-11T>C
XM_005254228.2:c.971-11T>C	XP_005254285.1:n.971-11T>C
XM_011521363.1:c.1070-11T>C	XP_011519665.1:n.1070-11T>C
XM_005254228.3:c.971-11T>C	XP_005254285.1:n.971-11T>C
XM_011521363.2:c.1070-11T>C	XP_011519665.1:n.1070-11T>C
NM_001004439.2:c.1277-11T>C MANE Select	NP_001004439.1:n.1277-11T>C