Canonical Allele Identifier: CA2184934393

Gene: ITGA11

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68335869_68335873delinsATCTT , CM000677.2:g.68335869_68335873delinsATCTT	GRCh38
NC_000015.9:g.68628207_68628211delinsATCTT , CM000677.1:g.68628207_68628211delinsATCTT	GRCh37
NC_000015.8:g.66415261_66415265delinsATCTT	NCBI36
NG_046911.1:g.101288_101292delinsAAGAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315757.9:c.1277-28_1277-24delinsAAGAT MANE Select	ENSP00000327290.7:n.1277-28_1277-24delinsAAGAT
ENST00000315757.8:c.1277-28_1277-24delinsAAGAT	ENSP00000327290.7:n.1277-28_1277-24delinsAAGAT
ENST00000423218.6:c.1277-28_1277-24delinsAAGAT	ENSP00000403392.2:n.1277-28_1277-24delinsAAGAT
ENST00000566429.1:n.197-59_197-55delinsAAGAT
ENST00000569346.5:n.228_232delinsAAGAT
NM_001004439.1:c.1277-28_1277-24delinsAAGAT	NP_001004439.1:n.1277-28_1277-24delinsAAGAT
XM_005254228.2:c.971-28_971-24delinsAAGAT	XP_005254285.1:n.971-28_971-24delinsAAGAT
XM_011521363.1:c.1070-28_1070-24delinsAAGAT	XP_011519665.1:n.1070-28_1070-24delinsAAGAT
XM_005254228.3:c.971-28_971-24delinsAAGAT	XP_005254285.1:n.971-28_971-24delinsAAGAT
XM_011521363.2:c.1070-28_1070-24delinsAAGAT	XP_011519665.1:n.1070-28_1070-24delinsAAGAT
NM_001004439.2:c.1277-28_1277-24delinsAAGAT MANE Select	NP_001004439.1:n.1277-28_1277-24delinsAAGAT