Canonical Allele Identifier: CA1307810894

Gene: ITGA6

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.172446710_172446711delinsGC , CM000664.2:g.172446710_172446711delinsGC	GRCh38
NC_000002.11:g.173311438_173311439delinsGC , CM000664.1:g.173311438_173311439delinsGC	GRCh37
NC_000002.10:g.173019684_173019685delinsGC	NCBI36
NG_008853.1:g.24125_24126delinsGC

Transcript Alleles

HGVS	Amino-acid change
ENST00000264107.12:c.182+18740_182+18741delinsGC	ENSP00000264107.8:n.182+18740_182+18741de...
ENST00000442250.6:c.182+18740_182+18741delinsGC MANE Plus Clinical	ENSP00000406694.1:n.182+18740_182+18741de...
ENST00000684293.1:c.182+18740_182+18741delinsGC MANE Select	ENSP00000508249.1:n.182+18740_182+18741de...
ENST00000409080.6:c.182+18740_182+18741delinsGC	ENSP00000386896.1:n.182+18740_182+18741de...
ENST00000264107.11:c.182+18740_182+18741delinsGC	ENSP00000264107.7:n.182+18740_182+18741de...
ENST00000409080.5:c.182+18740_182+18741delinsGC	ENSP00000386896.1:n.182+18740_182+18741de...
ENST00000409532.5:c.-160-18829_-160-18828delinsGC	ENSP00000386614.1:n.-160-18829_-160-18828...
ENST00000412899.5:c.-160-18829_-160-18828delinsGC	ENSP00000413470.1:n.-160-18829_-160-18828...
ENST00000442250.5:c.182+18740_182+18741delinsGC	ENSP00000406694.1:n.182+18740_182+18741de...
ENST00000458358.5:c.182+18740_182+18741delinsGC	ENSP00000394169.1:n.182+18740_182+18741de...
NM_000210.2:c.182+18740_182+18741delinsGC	NP_000201.2:n.182+18740_182+18741delinsGC...
NM_000210.3:c.182+18740_182+18741delinsGC	NP_000201.2:n.182+18740_182+18741delinsGC...
NM_001079818.1:c.182+18740_182+18741delinsGC	NP_001073286.1:n.182+18740_182+18741delin...
NM_001079818.2:c.182+18740_182+18741delinsGC	NP_001073286.1:n.182+18740_182+18741delin...
NM_001316306.1:c.-160-18829_-160-18828delinsGC	NP_001303235.1:n.-160-18829_-160-18828del...
XM_006712510.1:c.182+18740_182+18741delinsGC	XP_006712573.1:n.182+18740_182+18741delin...
XM_006712511.1:c.182+18740_182+18741delinsGC	XP_006712574.1:n.182+18740_182+18741delin...
NM_001365529.1:c.182+18740_182+18741delinsGC	NP_001352458.1:n.182+18740_182+18741delin...
NM_001365530.1:c.182+18740_182+18741delinsGC	NP_001352459.1:n.182+18740_182+18741delin...
XM_017004005.1:c.-160-18829_-160-18828delinsGC	XP_016859494.1:n.-160-18829_-160-18828del...
XM_017004006.1:c.-160-18829_-160-18828delinsGC	XP_016859495.1:n.-160-18829_-160-18828del...
XM_017004007.1:c.-160-18829_-160-18828delinsGC	XP_016859496.1:n.-160-18829_-160-18828del...
XM_017004008.1:c.-160-18829_-160-18828delinsGC	XP_016859497.1:n.-160-18829_-160-18828del...
NM_001079818.3:c.182+18740_182+18741delinsGC	NP_001073286.1:n.182+18740_182+18741delin...
NM_000210.4:c.182+18740_182+18741delinsGC MANE Select	NP_000201.2:n.182+18740_182+18741delinsGC...
NM_001316306.2:c.-160-18829_-160-18828delinsGC	NP_001303235.1:n.-160-18829_-160-18828del...
NM_001365529.2:c.182+18740_182+18741delinsGC	NP_001352458.1:n.182+18740_182+18741delin...
NM_001365530.2:c.182+18740_182+18741delinsGC	NP_001352459.1:n.182+18740_182+18741delin...
NM_001394928.1:c.182+18740_182+18741delinsGC MANE Plus Clinical	NP_001381857.1:n.182+18740_182+18741delin...