Canonical Allele Identifier: CA916711265

Gene: ITGA6 ITGA6-AS1

Linked Data

• ClinVar Variation Id: 2807846
• ClinVar RCV Id: RCV003684538
• dbSNP Id: rs1574365202

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.172467576_172467577del , CM000664.2:g.172467576_172467577del	GRCh38
NC_000002.11:g.173332304_173332305del , CM000664.1:g.173332304_173332305del	GRCh37
NC_000002.10:g.173040550_173040551del	NCBI36
NG_008853.1:g.44991_44992del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264107.12:c.387+16_387+17del (ITGA6)	ENSP00000264107.8:n.387+16_387+17del
ENST00000442250.6:c.387+16_387+17del (ITGA6) MANE Plus Clinical	ENSP00000406694.1:n.387+16_387+17del
ENST00000684293.1:c.387+16_387+17del (ITGA6) MANE Select	ENSP00000508249.1:n.387+16_387+17del
ENST00000409080.6:c.387+16_387+17del (ITGA6)	ENSP00000386896.1:n.387+16_387+17del
ENST00000264107.11:c.387+16_387+17del (ITGA6)	ENSP00000264107.7:n.387+16_387+17del
ENST00000409080.5:c.387+16_387+17del (ITGA6)	ENSP00000386896.1:n.387+16_387+17del
ENST00000409532.5:c.45+16_45+17del (ITGA6)	ENSP00000386614.1:n.45+16_45+17del
ENST00000412899.5:c.45+16_45+17del (ITGA6)	ENSP00000413470.1:n.45+16_45+17del
ENST00000442250.5:c.387+16_387+17del (ITGA6)	ENSP00000406694.1:n.387+16_387+17del
ENST00000458358.5:c.387+16_387+17del (ITGA6)	ENSP00000394169.1:n.387+16_387+17del
NM_000210.2:c.387+16_387+17del (ITGA6)	NP_000201.2:n.387+16_387+17del
NM_000210.3:c.387+16_387+17del (ITGA6)	NP_000201.2:n.387+16_387+17del
NM_001079818.1:c.387+16_387+17del (ITGA6)	NP_001073286.1:n.387+16_387+17del
NM_001079818.2:c.387+16_387+17del (ITGA6)	NP_001073286.1:n.387+16_387+17del
NM_001316306.1:c.45+16_45+17del (ITGA6)	NP_001303235.1:n.45+16_45+17del
XM_006712510.1:c.387+16_387+17del (ITGA6)	XP_006712573.1:n.387+16_387+17del
XM_006712511.1:c.387+16_387+17del (ITGA6)	XP_006712574.1:n.387+16_387+17del
NM_001365529.1:c.387+16_387+17del (ITGA6)	NP_001352458.1:n.387+16_387+17del
NM_001365530.1:c.387+16_387+17del (ITGA6)	NP_001352459.1:n.387+16_387+17del
XM_017004005.1:c.45+16_45+17del (ITGA6)	XP_016859494.1:n.45+16_45+17del
XM_017004006.1:c.45+16_45+17del (ITGA6)	XP_016859495.1:n.45+16_45+17del
XM_017004007.1:c.45+16_45+17del (ITGA6)	XP_016859496.1:n.45+16_45+17del
XM_017004008.1:c.45+16_45+17del (ITGA6)	XP_016859497.1:n.45+16_45+17del
XR_001739781.1:n.410-3000_410-2999del (ITGA6-AS1)
XR_001739782.1:n.410-1553_410-1552del (ITGA6-AS1)
XR_001739784.1:n.410-1553_410-1552del (ITGA6-AS1)
XR_001739785.1:n.410-1553_410-1552del (ITGA6-AS1)
XR_001739786.1:n.521-1553_521-1552del (ITGA6-AS1)
XR_001739788.1:n.505-3000_505-2999del (ITGA6-AS1)
NM_001079818.3:c.387+16_387+17del (ITGA6)	NP_001073286.1:n.387+16_387+17del
NM_000210.4:c.387+16_387+17del (ITGA6) MANE Select	NP_000201.2:n.387+16_387+17del
NM_001316306.2:c.45+16_45+17del (ITGA6)	NP_001303235.1:n.45+16_45+17del
NM_001365529.2:c.387+16_387+17del (ITGA6)	NP_001352458.1:n.387+16_387+17del
NM_001365530.2:c.387+16_387+17del (ITGA6)	NP_001352459.1:n.387+16_387+17del
NM_001394928.1:c.387+16_387+17del (ITGA6) MANE Plus Clinical	NP_001381857.1:n.387+16_387+17del