Canonical Allele Identifier: CA2038036066
Gene: ITGA7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.55693308G= , CM000674.2:g.55693308G= GRCh38
NC_000012.11:g.56087092G= , CM000674.1:g.56087092G= GRCh37
NC_000012.10:g.54373359G= NCBI36
NG_012343.1:g.23998C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000553893.6:c.*2169C= ENSP00000452467.1:n.*2169C=
ENST00000554327.6:c.1216C=
ENST00000557058.2:n.1960C=
ENST00000557257.2:c.2071C= ENSP00000450578.2:p.Gln691=
ENST00000557555.3:c.2557C= ENSP00000451039.3:p.Gln853=
ENST00000686981.1:c.*2256C= ENSP00000510795.1:n.*2256C=
ENST00000687390.1:n.651C=
ENST00000691052.1:c.*1029C= ENSP00000508886.1:n.*1029C=
ENST00000691846.1:c.1358C=
ENST00000691973.1:c.2557C= ENSP00000509141.1:p.Gln853=
ENST00000257879.11:c.2545C= MANE Select ENSP00000257879.7:p.Gln849=
ENST00000553804.6:c.2557C= ENSP00000452120.1:p.Gln853=
ENST00000257879.10:c.2545C= ENSP00000257879.6:p.Gln849=
ENST00000347027.10:c.2527C= ENSP00000343009.6:p.Gln843=
ENST00000452168.6:c.2266C= ENSP00000393844.2:p.Gln756=
ENST00000553804.5:c.2557C= ENSP00000452120.1:p.Gln853=
ENST00000554327.5:c.610C=
ENST00000555728.5:c.2677C= ENSP00000452387.1:p.Gln893=
NM_001144996.1:c.2557C= NP_001138468.1:p.Gln853=
NM_001144997.1:c.2266C= NP_001138469.1:p.Gln756=
NM_002206.2:c.2545C= NP_002197.2:p.Gln849=
XM_005268839.1:c.2677C= XP_005268896.1:p.Gln893=
XM_005268840.1:c.2659C= XP_005268897.1:p.Gln887=
XM_005268841.1:c.2677C= XP_005268898.1:p.Gln893=
XM_005268842.1:c.2527C= XP_005268899.1:p.Gln843=
XM_005268844.1:c.2338C= XP_005268901.1:p.Gln780=
XM_005268845.1:c.2206C= XP_005268902.1:p.Gln736=
XM_005268846.1:c.2206C= XP_005268903.1:p.Gln736=
XM_005268847.1:c.2203C= XP_005268904.1:p.Gln735=
XM_005268848.1:c.2203C= XP_005268905.1:p.Gln735=
XM_005268849.1:c.2203C= XP_005268906.1:p.Gln735=
XM_005268850.1:c.2071C= XP_005268907.1:p.Gln691=
XM_011538286.1:c.2338C= XP_011536588.1:p.Gln780=
XM_005268839.2:c.2677C= XP_005268896.1:p.Gln893=
XM_005268840.2:c.2659C= XP_005268897.1:p.Gln887=
XM_005268841.2:c.2677C= XP_005268898.1:p.Gln893=
XM_005268842.2:c.2527C= XP_005268899.1:p.Gln843=
XM_017019265.1:c.2287C= XP_016874754.1:p.Gln763=
NM_001144996.2:c.2557C= NP_001138468.1:p.Gln853=
NM_001367993.1:c.2218C= NP_001354922.1:p.Gln740=
NM_001367994.1:c.1201C= NP_001354923.1:p.Gln401=
NM_001374465.1:c.2527C= NP_001361394.1:p.Gln843=
NM_002206.3:c.2545C= MANE Select NP_002197.2:p.Gln849=