Canonical Allele Identifier: CA392977772

Gene: ITGA11

Linked Data

• gnomAD v4: 15-68335750-T-C
• MyVariant Identifiers: chr15:g.68628088T>C (hg19) ; chr15:g.68335750T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68335750T>C , CM000677.2:g.68335750T>C	GRCh38
NC_000015.9:g.68628088T>C , CM000677.1:g.68628088T>C	GRCh37
NC_000015.8:g.66415142T>C	NCBI36
NG_046911.1:g.101411A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315757.9:c.1372A>G MANE Select	ENSP00000327290.7:p.Thr458Ala
ENST00000315757.8:c.1372A>G	ENSP00000327290.7:p.Thr458Ala
ENST00000423218.6:c.1372A>G	ENSP00000403392.2:p.Thr458Ala
ENST00000566429.1:n.261A>G
ENST00000569346.5:n.351A>G
NM_001004439.1:c.1372A>G	NP_001004439.1:p.Thr458Ala
XM_005254228.2:c.1066A>G	XP_005254285.1:p.Thr356Ala
XM_011521363.1:c.1165A>G	XP_011519665.1:p.Thr389Ala
XM_005254228.3:c.1066A>G	XP_005254285.1:p.Thr356Ala
XM_011521363.2:c.1165A>G	XP_011519665.1:p.Thr389Ala
NM_001004439.2:c.1372A>G MANE Select	NP_001004439.1:p.Thr458Ala