Canonical Allele Identifier: CA11342393
Gene: ITGA6 HGNC NCBI

Linked Data

dbSNP Id: rs13027811

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.172435945A>G , CM000664.2:g.172435945A>G GRCh38
NC_000002.11:g.173300673A>G , CM000664.1:g.173300673A>G GRCh37
NC_000002.10:g.173008919A>G NCBI36
NG_008853.1:g.13360A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000264107.12:c.182+7975A>G ENSP00000264107.8:n.182+7975A>G
ENST00000442250.6:c.182+7975A>G MANE Plus Clinical ENSP00000406694.1:n.182+7975A>G
ENST00000684293.1:c.182+7975A>G MANE Select ENSP00000508249.1:n.182+7975A>G
ENST00000409080.6:c.182+7975A>G ENSP00000386896.1:n.182+7975A>G
ENST00000264107.11:c.182+7975A>G ENSP00000264107.7:n.182+7975A>G
ENST00000409080.5:c.182+7975A>G ENSP00000386896.1:n.182+7975A>G
ENST00000409532.5:c.-161+8475A>G ENSP00000386614.1:n.-161+8475A>G
ENST00000412899.5:c.-161+8475A>G ENSP00000413470.1:n.-161+8475A>G
ENST00000442250.5:c.182+7975A>G ENSP00000406694.1:n.182+7975A>G
ENST00000458358.5:c.182+7975A>G ENSP00000394169.1:n.182+7975A>G
NM_000210.2:c.182+7975A>G NP_000201.2:n.182+7975A>G
NM_000210.3:c.182+7975A>G NP_000201.2:n.182+7975A>G
NM_001079818.1:c.182+7975A>G NP_001073286.1:n.182+7975A>G
NM_001079818.2:c.182+7975A>G NP_001073286.1:n.182+7975A>G
NM_001316306.1:c.-161+8475A>G NP_001303235.1:n.-161+8475A>G
XM_006712510.1:c.182+7975A>G XP_006712573.1:n.182+7975A>G
XM_006712511.1:c.182+7975A>G XP_006712574.1:n.182+7975A>G
NM_001365529.1:c.182+7975A>G NP_001352458.1:n.182+7975A>G
NM_001365530.1:c.182+7975A>G NP_001352459.1:n.182+7975A>G
XM_017004005.1:c.-161+8475A>G XP_016859494.1:n.-161+8475A>G
XM_017004006.1:c.-161+8475A>G XP_016859495.1:n.-161+8475A>G
XM_017004007.1:c.-161+8475A>G XP_016859496.1:n.-161+8475A>G
XM_017004008.1:c.-161+8475A>G XP_016859497.1:n.-161+8475A>G
NM_001079818.3:c.182+7975A>G NP_001073286.1:n.182+7975A>G
NM_000210.4:c.182+7975A>G MANE Select NP_000201.2:n.182+7975A>G
NM_001316306.2:c.-161+8475A>G NP_001303235.1:n.-161+8475A>G
NM_001365529.2:c.182+7975A>G NP_001352458.1:n.182+7975A>G
NM_001365530.2:c.182+7975A>G NP_001352459.1:n.182+7975A>G
NM_001394928.1:c.182+7975A>G MANE Plus Clinical NP_001381857.1:n.182+7975A>G