Canonical Allele Identifier: CA392977920

Gene: ITGA11

Linked Data

• MyVariant Identifiers: chr15:g.68628163C>A (hg19) ; chr15:g.68335825C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68335825C>A , CM000677.2:g.68335825C>A	GRCh38
NC_000015.9:g.68628163C>A , CM000677.1:g.68628163C>A	GRCh37
NC_000015.8:g.66415217C>A	NCBI36
NG_046911.1:g.101336G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000315757.9:c.1297G>T MANE Select	ENSP00000327290.7:p.Val433Leu
ENST00000315757.8:c.1297G>T	ENSP00000327290.7:p.Val433Leu
ENST00000423218.6:c.1297G>T	ENSP00000403392.2:p.Val433Leu
ENST00000566429.1:n.197-11G>T
ENST00000569346.5:n.276G>T
NM_001004439.1:c.1297G>T	NP_001004439.1:p.Val433Leu
XM_005254228.2:c.991G>T	XP_005254285.1:p.Val331Leu
XM_011521363.1:c.1090G>T	XP_011519665.1:p.Val364Leu
XM_005254228.3:c.991G>T	XP_005254285.1:p.Val331Leu
XM_011521363.2:c.1090G>T	XP_011519665.1:p.Val364Leu
NM_001004439.2:c.1297G>T MANE Select	NP_001004439.1:p.Val433Leu