Canonical Allele Identifier: CA2038035760
Gene: ITGA7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.55693184C= , CM000674.2:g.55693184C= GRCh38
NC_000012.11:g.56086968C= , CM000674.1:g.56086968C= GRCh37
NC_000012.10:g.54373235C= NCBI36
NG_012343.1:g.24122G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000553893.6:c.*2293G= ENSP00000452467.1:n.*2293G=
ENST00000554327.6:c.1340G=
ENST00000557058.2:n.2084G=
ENST00000557257.2:c.2195G= ENSP00000450578.2:p.Gly732=
ENST00000557555.3:c.2681G= ENSP00000451039.3:p.Gly894=
ENST00000686981.1:c.*2380G= ENSP00000510795.1:n.*2380G=
ENST00000687390.1:n.775G=
ENST00000691052.1:c.*1153G= ENSP00000508886.1:n.*1153G=
ENST00000691846.1:c.1482G=
ENST00000691973.1:c.2652+29G= ENSP00000509141.1:n.2652+29G=
ENST00000257879.11:c.2669G= MANE Select ENSP00000257879.7:p.Gly890=
ENST00000553804.6:c.2681G= ENSP00000452120.1:p.Gly894=
ENST00000257879.10:c.2669G= ENSP00000257879.6:p.Gly890=
ENST00000347027.10:c.2651G= ENSP00000343009.6:p.Gly884=
ENST00000452168.6:c.2390G= ENSP00000393844.2:p.Gly797=
ENST00000553804.5:c.2681G= ENSP00000452120.1:p.Gly894=
ENST00000554327.5:c.734G=
ENST00000555728.5:c.2801G= ENSP00000452387.1:p.Gly934=
NM_001144996.1:c.2681G= NP_001138468.1:p.Gly894=
NM_001144997.1:c.2390G= NP_001138469.1:p.Gly797=
NM_002206.2:c.2669G= NP_002197.2:p.Gly890=
XM_005268839.1:c.2801G= XP_005268896.1:p.Gly934=
XM_005268840.1:c.2783G= XP_005268897.1:p.Gly928=
XM_005268841.1:c.2801G= XP_005268898.1:p.Gly934=
XM_005268842.1:c.2651G= XP_005268899.1:p.Gly884=
XM_005268844.1:c.2462G= XP_005268901.1:p.Gly821=
XM_005268845.1:c.2330G= XP_005268902.1:p.Gly777=
XM_005268846.1:c.2330G= XP_005268903.1:p.Gly777=
XM_005268847.1:c.2327G= XP_005268904.1:p.Gly776=
XM_005268848.1:c.2327G= XP_005268905.1:p.Gly776=
XM_005268849.1:c.2327G= XP_005268906.1:p.Gly776=
XM_005268850.1:c.2195G= XP_005268907.1:p.Gly732=
XM_011538286.1:c.2462G= XP_011536588.1:p.Gly821=
XM_005268839.2:c.2801G= XP_005268896.1:p.Gly934=
XM_005268840.2:c.2783G= XP_005268897.1:p.Gly928=
XM_005268841.2:c.2801G= XP_005268898.1:p.Gly934=
XM_005268842.2:c.2651G= XP_005268899.1:p.Gly884=
XM_017019265.1:c.2411G= XP_016874754.1:p.Gly804=
NM_001144996.2:c.2681G= NP_001138468.1:p.Gly894=
NM_001367993.1:c.2342G= NP_001354922.1:p.Gly781=
NM_001367994.1:c.1325G= NP_001354923.1:p.Gly442=
NM_001374465.1:c.2651G= NP_001361394.1:p.Gly884=
NM_002206.3:c.2669G= MANE Select NP_002197.2:p.Gly890=