Canonical Allele Identifier: CA2038035966
Gene: ITGA7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.55693267G= , CM000674.2:g.55693267G= GRCh38
NC_000012.11:g.56087051G= , CM000674.1:g.56087051G= GRCh37
NC_000012.10:g.54373318G= NCBI36
NG_012343.1:g.24039C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000553893.6:c.*2210C= ENSP00000452467.1:n.*2210C=
ENST00000554327.6:c.1257C=
ENST00000557058.2:n.2001C=
ENST00000557257.2:c.2112C= ENSP00000450578.2:p.Asn704=
ENST00000557555.3:c.2598C= ENSP00000451039.3:p.Asn866=
ENST00000686981.1:c.*2297C= ENSP00000510795.1:n.*2297C=
ENST00000687390.1:n.692C=
ENST00000691052.1:c.*1070C= ENSP00000508886.1:n.*1070C=
ENST00000691846.1:c.1399C=
ENST00000691973.1:c.2598C= ENSP00000509141.1:p.Asn866=
ENST00000257879.11:c.2586C= MANE Select ENSP00000257879.7:p.Asn862=
ENST00000553804.6:c.2598C= ENSP00000452120.1:p.Asn866=
ENST00000257879.10:c.2586C= ENSP00000257879.6:p.Asn862=
ENST00000347027.10:c.2568C= ENSP00000343009.6:p.Asn856=
ENST00000452168.6:c.2307C= ENSP00000393844.2:p.Asn769=
ENST00000553804.5:c.2598C= ENSP00000452120.1:p.Asn866=
ENST00000554327.5:c.651C=
ENST00000555728.5:c.2718C= ENSP00000452387.1:p.Asn906=
NM_001144996.1:c.2598C= NP_001138468.1:p.Asn866=
NM_001144997.1:c.2307C= NP_001138469.1:p.Asn769=
NM_002206.2:c.2586C= NP_002197.2:p.Asn862=
XM_005268839.1:c.2718C= XP_005268896.1:p.Asn906=
XM_005268840.1:c.2700C= XP_005268897.1:p.Asn900=
XM_005268841.1:c.2718C= XP_005268898.1:p.Asn906=
XM_005268842.1:c.2568C= XP_005268899.1:p.Asn856=
XM_005268844.1:c.2379C= XP_005268901.1:p.Asn793=
XM_005268845.1:c.2247C= XP_005268902.1:p.Asn749=
XM_005268846.1:c.2247C= XP_005268903.1:p.Asn749=
XM_005268847.1:c.2244C= XP_005268904.1:p.Asn748=
XM_005268848.1:c.2244C= XP_005268905.1:p.Asn748=
XM_005268849.1:c.2244C= XP_005268906.1:p.Asn748=
XM_005268850.1:c.2112C= XP_005268907.1:p.Asn704=
XM_011538286.1:c.2379C= XP_011536588.1:p.Asn793=
XM_005268839.2:c.2718C= XP_005268896.1:p.Asn906=
XM_005268840.2:c.2700C= XP_005268897.1:p.Asn900=
XM_005268841.2:c.2718C= XP_005268898.1:p.Asn906=
XM_005268842.2:c.2568C= XP_005268899.1:p.Asn856=
XM_017019265.1:c.2328C= XP_016874754.1:p.Asn776=
NM_001144996.2:c.2598C= NP_001138468.1:p.Asn866=
NM_001367993.1:c.2259C= NP_001354922.1:p.Asn753=
NM_001367994.1:c.1242C= NP_001354923.1:p.Asn414=
NM_001374465.1:c.2568C= NP_001361394.1:p.Asn856=
NM_002206.3:c.2586C= MANE Select NP_002197.2:p.Asn862=