Canonical Allele Identifier: CA2575182696

Gene: ITGA7

Linked Data

• gnomAD v4: 12-55693255-AG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.55693257del , CM000674.2:g.55693257del	GRCh38
NC_000012.11:g.56087041del , CM000674.1:g.56087041del	GRCh37
NC_000012.10:g.54373308del	NCBI36
NG_012343.1:g.24050del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553893.6:c.*2221del	ENSP00000452467.1:n.*2221del
ENST00000554327.6:c.1268del
ENST00000557058.2:n.2012del
ENST00000557257.2:c.2123del	ENSP00000450578.2:p.Pro708LeufsTer?
ENST00000557555.3:c.2609del	ENSP00000451039.3:p.Pro870LeufsTer?
ENST00000686981.1:c.*2308del	ENSP00000510795.1:n.*2308del
ENST00000687390.1:n.703del
ENST00000691052.1:c.*1081del	ENSP00000508886.1:n.*1081del
ENST00000691846.1:c.1410del
ENST00000691973.1:c.2609del	ENSP00000509141.1:p.Pro870LeufsTer?
ENST00000257879.11:c.2597del MANE Select	ENSP00000257879.7:p.Pro866LeufsTer?
ENST00000553804.6:c.2609del	ENSP00000452120.1:p.Pro870LeufsTer?
ENST00000257879.10:c.2597del	ENSP00000257879.6:p.Pro866LeufsTer?
ENST00000347027.10:c.2579del	ENSP00000343009.6:p.Pro860LeufsTer?
ENST00000452168.6:c.2318del	ENSP00000393844.2:p.Pro773LeufsTer?
ENST00000553804.5:c.2609del	ENSP00000452120.1:p.Pro870LeufsTer?
ENST00000554327.5:c.662del
ENST00000555728.5:c.2729del	ENSP00000452387.1:p.Pro910LeufsTer?
NM_001144996.1:c.2609del	NP_001138468.1:p.Pro870LeufsTer?
NM_001144997.1:c.2318del	NP_001138469.1:p.Pro773LeufsTer?
NM_002206.2:c.2597del	NP_002197.2:p.Pro866LeufsTer?
XM_005268839.1:c.2729del	XP_005268896.1:p.Pro910LeufsTer?
XM_005268840.1:c.2711del	XP_005268897.1:p.Pro904LeufsTer?
XM_005268841.1:c.2729del	XP_005268898.1:p.Pro910LeufsTer?
XM_005268842.1:c.2579del	XP_005268899.1:p.Pro860LeufsTer?
XM_005268844.1:c.2390del	XP_005268901.1:p.Pro797LeufsTer?
XM_005268845.1:c.2258del	XP_005268902.1:p.Pro753LeufsTer?
XM_005268846.1:c.2258del	XP_005268903.1:p.Pro753LeufsTer?
XM_005268847.1:c.2255del	XP_005268904.1:p.Pro752LeufsTer?
XM_005268848.1:c.2255del	XP_005268905.1:p.Pro752LeufsTer?
XM_005268849.1:c.2255del	XP_005268906.1:p.Pro752LeufsTer?
XM_005268850.1:c.2123del	XP_005268907.1:p.Pro708LeufsTer?
XM_011538286.1:c.2390del	XP_011536588.1:p.Pro797LeufsTer?
XM_005268839.2:c.2729del	XP_005268896.1:p.Pro910LeufsTer?
XM_005268840.2:c.2711del	XP_005268897.1:p.Pro904LeufsTer?
XM_005268841.2:c.2729del	XP_005268898.1:p.Pro910LeufsTer?
XM_005268842.2:c.2579del	XP_005268899.1:p.Pro860LeufsTer?
XM_017019265.1:c.2339del	XP_016874754.1:p.Pro780LeufsTer?
NM_001144996.2:c.2609del	NP_001138468.1:p.Pro870LeufsTer?
NM_001367993.1:c.2270del	NP_001354922.1:p.Pro757LeufsTer?
NM_001367994.1:c.1253del	NP_001354923.1:p.Pro418LeufsTer?
NM_001374465.1:c.2579del	NP_001361394.1:p.Pro860LeufsTer?
NM_002206.3:c.2597del MANE Select	NP_002197.2:p.Pro866LeufsTer?