Canonical Allele Identifier: CA392977809

Gene: ITGA11

Linked Data

• MyVariant Identifiers: chr15:g.68628106C>T (hg19) ; chr15:g.68335768C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68335768C>T , CM000677.2:g.68335768C>T	GRCh38
NC_000015.9:g.68628106C>T , CM000677.1:g.68628106C>T	GRCh37
NC_000015.8:g.66415160C>T	NCBI36
NG_046911.1:g.101393G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315757.9:c.1354G>A MANE Select	ENSP00000327290.7:p.Gly452Ser
ENST00000315757.8:c.1354G>A	ENSP00000327290.7:p.Gly452Ser
ENST00000423218.6:c.1354G>A	ENSP00000403392.2:p.Gly452Ser
ENST00000566429.1:n.243G>A
ENST00000569346.5:n.333G>A
NM_001004439.1:c.1354G>A	NP_001004439.1:p.Gly452Ser
XM_005254228.2:c.1048G>A	XP_005254285.1:p.Gly350Ser
XM_011521363.1:c.1147G>A	XP_011519665.1:p.Gly383Ser
XM_005254228.3:c.1048G>A	XP_005254285.1:p.Gly350Ser
XM_011521363.2:c.1147G>A	XP_011519665.1:p.Gly383Ser
NM_001004439.2:c.1354G>A MANE Select	NP_001004439.1:p.Gly452Ser