Canonical Allele Identifier: CA2038036058
Gene: ITGA7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.55693303G= , CM000674.2:g.55693303G= GRCh38
NC_000012.11:g.56087087G= , CM000674.1:g.56087087G= GRCh37
NC_000012.10:g.54373354G= NCBI36
NG_012343.1:g.24003C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000553893.6:c.*2174C= ENSP00000452467.1:n.*2174C=
ENST00000554327.6:c.1221C=
ENST00000557058.2:n.1965C=
ENST00000557257.2:c.2076C= ENSP00000450578.2:p.Gly692=
ENST00000557555.3:c.2562C= ENSP00000451039.3:p.Gly854=
ENST00000686981.1:c.*2261C= ENSP00000510795.1:n.*2261C=
ENST00000687390.1:n.656C=
ENST00000691052.1:c.*1034C= ENSP00000508886.1:n.*1034C=
ENST00000691846.1:c.1363C=
ENST00000691973.1:c.2562C= ENSP00000509141.1:p.Gly854=
ENST00000257879.11:c.2550C= MANE Select ENSP00000257879.7:p.Gly850=
ENST00000553804.6:c.2562C= ENSP00000452120.1:p.Gly854=
ENST00000257879.10:c.2550C= ENSP00000257879.6:p.Gly850=
ENST00000347027.10:c.2532C= ENSP00000343009.6:p.Gly844=
ENST00000452168.6:c.2271C= ENSP00000393844.2:p.Gly757=
ENST00000553804.5:c.2562C= ENSP00000452120.1:p.Gly854=
ENST00000554327.5:c.615C=
ENST00000555728.5:c.2682C= ENSP00000452387.1:p.Gly894=
NM_001144996.1:c.2562C= NP_001138468.1:p.Gly854=
NM_001144997.1:c.2271C= NP_001138469.1:p.Gly757=
NM_002206.2:c.2550C= NP_002197.2:p.Gly850=
XM_005268839.1:c.2682C= XP_005268896.1:p.Gly894=
XM_005268840.1:c.2664C= XP_005268897.1:p.Gly888=
XM_005268841.1:c.2682C= XP_005268898.1:p.Gly894=
XM_005268842.1:c.2532C= XP_005268899.1:p.Gly844=
XM_005268844.1:c.2343C= XP_005268901.1:p.Gly781=
XM_005268845.1:c.2211C= XP_005268902.1:p.Gly737=
XM_005268846.1:c.2211C= XP_005268903.1:p.Gly737=
XM_005268847.1:c.2208C= XP_005268904.1:p.Gly736=
XM_005268848.1:c.2208C= XP_005268905.1:p.Gly736=
XM_005268849.1:c.2208C= XP_005268906.1:p.Gly736=
XM_005268850.1:c.2076C= XP_005268907.1:p.Gly692=
XM_011538286.1:c.2343C= XP_011536588.1:p.Gly781=
XM_005268839.2:c.2682C= XP_005268896.1:p.Gly894=
XM_005268840.2:c.2664C= XP_005268897.1:p.Gly888=
XM_005268841.2:c.2682C= XP_005268898.1:p.Gly894=
XM_005268842.2:c.2532C= XP_005268899.1:p.Gly844=
XM_017019265.1:c.2292C= XP_016874754.1:p.Gly764=
NM_001144996.2:c.2562C= NP_001138468.1:p.Gly854=
NM_001367993.1:c.2223C= NP_001354922.1:p.Gly741=
NM_001367994.1:c.1206C= NP_001354923.1:p.Gly402=
NM_001374465.1:c.2532C= NP_001361394.1:p.Gly844=
NM_002206.3:c.2550C= MANE Select NP_002197.2:p.Gly850=