Canonical Allele Identifier: CA490946318

Gene: ITGA11

Linked Data

• gnomAD v4: 15-68335787-G-T
• MyVariant Identifiers: chr15:g.68628125G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68335787G>T , CM000677.2:g.68335787G>T	GRCh38
NC_000015.9:g.68628125G>T , CM000677.1:g.68628125G>T	GRCh37
NC_000015.8:g.66415179G>T	NCBI36
NG_046911.1:g.101374C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315757.9:c.1335C>A MANE Select	ENSP00000327290.7:p.Ala445=
ENST00000315757.8:c.1335C>A	ENSP00000327290.7:p.Ala445=
ENST00000423218.6:c.1335C>A	ENSP00000403392.2:p.Ala445=
ENST00000566429.1:n.224C>A
ENST00000569346.5:n.314C>A
NM_001004439.1:c.1335C>A	NP_001004439.1:p.Ala445=
XM_005254228.2:c.1029C>A	XP_005254285.1:p.Ala343=
XM_011521363.1:c.1128C>A	XP_011519665.1:p.Ala376=
XM_005254228.3:c.1029C>A	XP_005254285.1:p.Ala343=
XM_011521363.2:c.1128C>A	XP_011519665.1:p.Ala376=
NM_001004439.2:c.1335C>A MANE Select	NP_001004439.1:p.Ala445=