Canonical Allele Identifier: CA490946312

Gene: ITGA11

Linked Data

• MyVariant Identifiers: chr15:g.68628119C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68335781C>G , CM000677.2:g.68335781C>G	GRCh38
NC_000015.9:g.68628119C>G , CM000677.1:g.68628119C>G	GRCh37
NC_000015.8:g.66415173C>G	NCBI36
NG_046911.1:g.101380G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315757.9:c.1341G>C MANE Select	ENSP00000327290.7:p.Arg447=
ENST00000315757.8:c.1341G>C	ENSP00000327290.7:p.Arg447=
ENST00000423218.6:c.1341G>C	ENSP00000403392.2:p.Arg447=
ENST00000566429.1:n.230G>C
ENST00000569346.5:n.320G>C
NM_001004439.1:c.1341G>C	NP_001004439.1:p.Arg447=
XM_005254228.2:c.1035G>C	XP_005254285.1:p.Arg345=
XM_011521363.1:c.1134G>C	XP_011519665.1:p.Arg378=
XM_005254228.3:c.1035G>C	XP_005254285.1:p.Arg345=
XM_011521363.2:c.1134G>C	XP_011519665.1:p.Arg378=
NM_001004439.2:c.1341G>C MANE Select	NP_001004439.1:p.Arg447=