Canonical Allele Identifier: CA392977716

Gene: ITGA11

Linked Data

• MyVariant Identifiers: chr15:g.68628063G>T (hg19) ; chr15:g.68335725G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68335725G>T , CM000677.2:g.68335725G>T	GRCh38
NC_000015.9:g.68628063G>T , CM000677.1:g.68628063G>T	GRCh37
NC_000015.8:g.66415117G>T	NCBI36
NG_046911.1:g.101436C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315757.9:c.1397C>A MANE Select	ENSP00000327290.7:p.Thr466Asn
ENST00000315757.8:c.1397C>A	ENSP00000327290.7:p.Thr466Asn
ENST00000423218.6:c.1397C>A	ENSP00000403392.2:p.Thr466Asn
ENST00000566429.1:n.286C>A
ENST00000569346.5:n.376C>A
NM_001004439.1:c.1397C>A	NP_001004439.1:p.Thr466Asn
XM_005254228.2:c.1091C>A	XP_005254285.1:p.Thr364Asn
XM_011521363.1:c.1190C>A	XP_011519665.1:p.Thr397Asn
XM_005254228.3:c.1091C>A	XP_005254285.1:p.Thr364Asn
XM_011521363.2:c.1190C>A	XP_011519665.1:p.Thr397Asn
NM_001004439.2:c.1397C>A MANE Select	NP_001004439.1:p.Thr466Asn