Canonical Allele Identifier: CA7631847

Gene: ITGA11

Linked Data

• dbSNP Id: rs2306024
• ExAC: 15:68628049 T / G
• gnomAD v2: 15-68628049-T-G
• gnomAD v3: 15-68335711-T-G
• gnomAD v4: 15-68335711-T-G
• MyVariant Identifiers: chr15:g.68628049T>G (hg19) ; chr15:g.68335711T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68335711T>G , CM000677.2:g.68335711T>G	GRCh38
NC_000015.9:g.68628049T>G , CM000677.1:g.68628049T>G	GRCh37
NC_000015.8:g.66415103T>G	NCBI36
NG_046911.1:g.101450A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315757.9:c.1411A>C MANE Select	ENSP00000327290.7:p.Met471Leu
ENST00000315757.8:c.1411A>C	ENSP00000327290.7:p.Met471Leu
ENST00000423218.6:c.1411A>C	ENSP00000403392.2:p.Met471Leu
ENST00000566429.1:n.300A>C
ENST00000569346.5:n.390A>C
NM_001004439.1:c.1411A>C	NP_001004439.1:p.Met471Leu
XM_005254228.2:c.1105A>C	XP_005254285.1:p.Met369Leu
XM_011521363.1:c.1204A>C	XP_011519665.1:p.Met402Leu
XM_005254228.3:c.1105A>C	XP_005254285.1:p.Met369Leu
XM_011521363.2:c.1204A>C	XP_011519665.1:p.Met402Leu
NM_001004439.2:c.1411A>C MANE Select	NP_001004439.1:p.Met471Leu