Canonical Allele Identifier: CA392977861

Gene: ITGA11

Linked Data

• MyVariant Identifiers: chr15:g.68628133C>A (hg19) ; chr15:g.68335795C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68335795C>A , CM000677.2:g.68335795C>A	GRCh38
NC_000015.9:g.68628133C>A , CM000677.1:g.68628133C>A	GRCh37
NC_000015.8:g.66415187C>A	NCBI36
NG_046911.1:g.101366G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315757.9:c.1327G>T MANE Select	ENSP00000327290.7:p.Ala443Ser
ENST00000315757.8:c.1327G>T	ENSP00000327290.7:p.Ala443Ser
ENST00000423218.6:c.1327G>T	ENSP00000403392.2:p.Ala443Ser
ENST00000566429.1:n.216G>T
ENST00000569346.5:n.306G>T
NM_001004439.1:c.1327G>T	NP_001004439.1:p.Ala443Ser
XM_005254228.2:c.1021G>T	XP_005254285.1:p.Ala341Ser
XM_011521363.1:c.1120G>T	XP_011519665.1:p.Ala374Ser
XM_005254228.3:c.1021G>T	XP_005254285.1:p.Ala341Ser
XM_011521363.2:c.1120G>T	XP_011519665.1:p.Ala374Ser
NM_001004439.2:c.1327G>T MANE Select	NP_001004439.1:p.Ala443Ser