Canonical Allele Identifier: CA392977904

Gene: ITGA11

Linked Data

• MyVariant Identifiers: chr15:g.68628154T>C (hg19) ; chr15:g.68335816T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68335816T>C , CM000677.2:g.68335816T>C	GRCh38
NC_000015.9:g.68628154T>C , CM000677.1:g.68628154T>C	GRCh37
NC_000015.8:g.66415208T>C	NCBI36
NG_046911.1:g.101345A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315757.9:c.1306A>G MANE Select	ENSP00000327290.7:p.Arg436Gly
ENST00000315757.8:c.1306A>G	ENSP00000327290.7:p.Arg436Gly
ENST00000423218.6:c.1306A>G	ENSP00000403392.2:p.Arg436Gly
ENST00000566429.1:n.197-2A>G
ENST00000569346.5:n.285A>G
NM_001004439.1:c.1306A>G	NP_001004439.1:p.Arg436Gly
XM_005254228.2:c.1000A>G	XP_005254285.1:p.Arg334Gly
XM_011521363.1:c.1099A>G	XP_011519665.1:p.Arg367Gly
XM_005254228.3:c.1000A>G	XP_005254285.1:p.Arg334Gly
XM_011521363.2:c.1099A>G	XP_011519665.1:p.Arg367Gly
NM_001004439.2:c.1306A>G MANE Select	NP_001004439.1:p.Arg436Gly