Canonical Allele Identifier: CA605246984

Gene: ITGA7

Linked Data

• dbSNP Id: rs1240535138
• gnomAD v2: 12-56087044-A-ATCT
• gnomAD v4: 12-55693260-A-ATCT
• MyVariant Identifiers: chr12:g.56087044_56087045insTCT (hg19) ; chr12:g.55693260_55693261insTCT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.55693260_55693261insTCT , CM000674.2:g.55693260_55693261insTCT	GRCh38
NC_000012.11:g.56087044_56087045insTCT , CM000674.1:g.56087044_56087045insTCT	GRCh37
NC_000012.10:g.54373311_54373312insTCT	NCBI36
NG_012343.1:g.24045_24046insAGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553893.6:c.*2216_*2217insAGA	ENSP00000452467.1:n.*2216_*2217insAGA
ENST00000554327.6:c.1263_1264insAGA
ENST00000557058.2:n.2007_2008insAGA
ENST00000557257.2:c.2118_2119insAGA	ENSP00000450578.2:p.Met706_Trp707insArg
ENST00000557555.3:c.2604_2605insAGA	ENSP00000451039.3:p.Met868_Trp869insArg
ENST00000686981.1:c.*2303_*2304insAGA	ENSP00000510795.1:n.*2303_*2304insAGA
ENST00000687390.1:n.698_699insAGA
ENST00000691052.1:c.*1076_*1077insAGA	ENSP00000508886.1:n.*1076_*1077insAGA
ENST00000691846.1:c.1405_1406insAGA
ENST00000691973.1:c.2604_2605insAGA	ENSP00000509141.1:p.Met868_Trp869insArg
ENST00000257879.11:c.2592_2593insAGA MANE Select	ENSP00000257879.7:p.Met864_Trp865insArg
ENST00000553804.6:c.2604_2605insAGA	ENSP00000452120.1:p.Met868_Trp869insArg
ENST00000257879.10:c.2592_2593insAGA	ENSP00000257879.6:p.Met864_Trp865insArg
ENST00000347027.10:c.2574_2575insAGA	ENSP00000343009.6:p.Met858_Trp859insArg
ENST00000452168.6:c.2313_2314insAGA	ENSP00000393844.2:p.Met771_Trp772insArg
ENST00000553804.5:c.2604_2605insAGA	ENSP00000452120.1:p.Met868_Trp869insArg
ENST00000554327.5:c.657_658insAGA
ENST00000555728.5:c.2724_2725insAGA	ENSP00000452387.1:p.Met908_Trp909insArg
NM_001144996.1:c.2604_2605insAGA	NP_001138468.1:p.Met868_Trp869insArg
NM_001144997.1:c.2313_2314insAGA	NP_001138469.1:p.Met771_Trp772insArg
NM_002206.2:c.2592_2593insAGA	NP_002197.2:p.Met864_Trp865insArg
XM_005268839.1:c.2724_2725insAGA	XP_005268896.1:p.Met908_Trp909insArg
XM_005268840.1:c.2706_2707insAGA	XP_005268897.1:p.Met902_Trp903insArg
XM_005268841.1:c.2724_2725insAGA	XP_005268898.1:p.Met908_Trp909insArg
XM_005268842.1:c.2574_2575insAGA	XP_005268899.1:p.Met858_Trp859insArg
XM_005268844.1:c.2385_2386insAGA	XP_005268901.1:p.Met795_Trp796insArg
XM_005268845.1:c.2253_2254insAGA	XP_005268902.1:p.Met751_Trp752insArg
XM_005268846.1:c.2253_2254insAGA	XP_005268903.1:p.Met751_Trp752insArg
XM_005268847.1:c.2250_2251insAGA	XP_005268904.1:p.Met750_Trp751insArg
XM_005268848.1:c.2250_2251insAGA	XP_005268905.1:p.Met750_Trp751insArg
XM_005268849.1:c.2250_2251insAGA	XP_005268906.1:p.Met750_Trp751insArg
XM_005268850.1:c.2118_2119insAGA	XP_005268907.1:p.Met706_Trp707insArg
XM_011538286.1:c.2385_2386insAGA	XP_011536588.1:p.Met795_Trp796insArg
XM_005268839.2:c.2724_2725insAGA	XP_005268896.1:p.Met908_Trp909insArg
XM_005268840.2:c.2706_2707insAGA	XP_005268897.1:p.Met902_Trp903insArg
XM_005268841.2:c.2724_2725insAGA	XP_005268898.1:p.Met908_Trp909insArg
XM_005268842.2:c.2574_2575insAGA	XP_005268899.1:p.Met858_Trp859insArg
XM_017019265.1:c.2334_2335insAGA	XP_016874754.1:p.Met778_Trp779insArg
NM_001144996.2:c.2604_2605insAGA	NP_001138468.1:p.Met868_Trp869insArg
NM_001367993.1:c.2265_2266insAGA	NP_001354922.1:p.Met755_Trp756insArg
NM_001367994.1:c.1248_1249insAGA	NP_001354923.1:p.Met416_Trp417insArg
NM_001374465.1:c.2574_2575insAGA	NP_001361394.1:p.Met858_Trp859insArg
NM_002206.3:c.2592_2593insAGA MANE Select	NP_002197.2:p.Met864_Trp865insArg