Canonical Allele Identifier: CA537719790

Gene: ITGA6

Linked Data

• dbSNP Id: rs1559120069
• gnomAD v2: 2-173311301-TCCAAGTGTGTA-T
• gnomAD v3: 2-172446573-TCCAAGTGTGTA-T
• gnomAD v4: 2-172446573-TCCAAGTGTGTA-T
• MyVariant Identifiers: chr2:g.173311302_173311312del (hg19) ; chr2:g.172446574_172446584del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.172446575_172446585del , CM000664.2:g.172446575_172446585del	GRCh38
NC_000002.11:g.173311303_173311313del , CM000664.1:g.173311303_173311313del	GRCh37
NC_000002.10:g.173019549_173019559del	NCBI36
NG_008853.1:g.23990_24000del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264107.12:c.182+18605_182+18615del	ENSP00000264107.8:n.182+18605_182+18615del
ENST00000442250.6:c.182+18605_182+18615del MANE Plus Clinical	ENSP00000406694.1:n.182+18605_182+18615del
ENST00000684293.1:c.182+18605_182+18615del MANE Select	ENSP00000508249.1:n.182+18605_182+18615del
ENST00000409080.6:c.182+18605_182+18615del	ENSP00000386896.1:n.182+18605_182+18615del
ENST00000264107.11:c.182+18605_182+18615del	ENSP00000264107.7:n.182+18605_182+18615del
ENST00000409080.5:c.182+18605_182+18615del	ENSP00000386896.1:n.182+18605_182+18615del
ENST00000409532.5:c.-160-18964_-160-18954del	ENSP00000386614.1:n.-160-18964_-160-18954del
ENST00000412899.5:c.-160-18964_-160-18954del	ENSP00000413470.1:n.-160-18964_-160-18954del
ENST00000442250.5:c.182+18605_182+18615del	ENSP00000406694.1:n.182+18605_182+18615del
ENST00000458358.5:c.182+18605_182+18615del	ENSP00000394169.1:n.182+18605_182+18615del
NM_000210.2:c.182+18605_182+18615del	NP_000201.2:n.182+18605_182+18615del
NM_000210.3:c.182+18605_182+18615del	NP_000201.2:n.182+18605_182+18615del
NM_001079818.1:c.182+18605_182+18615del	NP_001073286.1:n.182+18605_182+18615del
NM_001079818.2:c.182+18605_182+18615del	NP_001073286.1:n.182+18605_182+18615del
NM_001316306.1:c.-160-18964_-160-18954del	NP_001303235.1:n.-160-18964_-160-18954del
XM_006712510.1:c.182+18605_182+18615del	XP_006712573.1:n.182+18605_182+18615del
XM_006712511.1:c.182+18605_182+18615del	XP_006712574.1:n.182+18605_182+18615del
NM_001365529.1:c.182+18605_182+18615del	NP_001352458.1:n.182+18605_182+18615del
NM_001365530.1:c.182+18605_182+18615del	NP_001352459.1:n.182+18605_182+18615del
XM_017004005.1:c.-160-18964_-160-18954del	XP_016859494.1:n.-160-18964_-160-18954del
XM_017004006.1:c.-160-18964_-160-18954del	XP_016859495.1:n.-160-18964_-160-18954del
XM_017004007.1:c.-160-18964_-160-18954del	XP_016859496.1:n.-160-18964_-160-18954del
XM_017004008.1:c.-160-18964_-160-18954del	XP_016859497.1:n.-160-18964_-160-18954del
NM_001079818.3:c.182+18605_182+18615del	NP_001073286.1:n.182+18605_182+18615del
NM_000210.4:c.182+18605_182+18615del MANE Select	NP_000201.2:n.182+18605_182+18615del
NM_001316306.2:c.-160-18964_-160-18954del	NP_001303235.1:n.-160-18964_-160-18954del
NM_001365529.2:c.182+18605_182+18615del	NP_001352458.1:n.182+18605_182+18615del
NM_001365530.2:c.182+18605_182+18615del	NP_001352459.1:n.182+18605_182+18615del
NM_001394928.1:c.182+18605_182+18615del MANE Plus Clinical	NP_001381857.1:n.182+18605_182+18615del