Canonical Allele Identifier: CA7631852

Gene: ITGA11

Linked Data

• dbSNP Id: rs765440239
• ExAC: 15:68628085 T / C
• gnomAD v2: 15-68628085-T-C
• gnomAD v3: 15-68335747-T-C
• gnomAD v4: 15-68335747-T-C
• MyVariant Identifiers: chr15:g.68628085T>C (hg19) ; chr15:g.68335747T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68335747T>C , CM000677.2:g.68335747T>C	GRCh38
NC_000015.9:g.68628085T>C , CM000677.1:g.68628085T>C	GRCh37
NC_000015.8:g.66415139T>C	NCBI36
NG_046911.1:g.101414A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315757.9:c.1375A>G MANE Select	ENSP00000327290.7:p.Met459Val
ENST00000315757.8:c.1375A>G	ENSP00000327290.7:p.Met459Val
ENST00000423218.6:c.1375A>G	ENSP00000403392.2:p.Met459Val
ENST00000566429.1:n.264A>G
ENST00000569346.5:n.354A>G
NM_001004439.1:c.1375A>G	NP_001004439.1:p.Met459Val
XM_005254228.2:c.1069A>G	XP_005254285.1:p.Met357Val
XM_011521363.1:c.1168A>G	XP_011519665.1:p.Met390Val
XM_005254228.3:c.1069A>G	XP_005254285.1:p.Met357Val
XM_011521363.2:c.1168A>G	XP_011519665.1:p.Met390Val
NM_001004439.2:c.1375A>G MANE Select	NP_001004439.1:p.Met459Val