Canonical Allele Identifier: CA392977925

Gene: ITGA11

Linked Data

• MyVariant Identifiers: chr15:g.68628166C>A (hg19) ; chr15:g.68335828C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68335828C>A , CM000677.2:g.68335828C>A	GRCh38
NC_000015.9:g.68628166C>A , CM000677.1:g.68628166C>A	GRCh37
NC_000015.8:g.66415220C>A	NCBI36
NG_046911.1:g.101333G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315757.9:c.1294G>T MANE Select	ENSP00000327290.7:p.Val432Phe
ENST00000315757.8:c.1294G>T	ENSP00000327290.7:p.Val432Phe
ENST00000423218.6:c.1294G>T	ENSP00000403392.2:p.Val432Phe
ENST00000566429.1:n.197-14G>T
ENST00000569346.5:n.273G>T
NM_001004439.1:c.1294G>T	NP_001004439.1:p.Val432Phe
XM_005254228.2:c.988G>T	XP_005254285.1:p.Val330Phe
XM_011521363.1:c.1087G>T	XP_011519665.1:p.Val363Phe
XM_005254228.3:c.988G>T	XP_005254285.1:p.Val330Phe
XM_011521363.2:c.1087G>T	XP_011519665.1:p.Val363Phe
NM_001004439.2:c.1294G>T MANE Select	NP_001004439.1:p.Val432Phe