Canonical Allele Identifier: CA10642858

Gene: ITGA7

Linked Data

• ClinVar Variation Id: 309775
• ClinVar RCV Id: RCV000286432
• dbSNP Id: rs886049663
• gnomAD v2: 12-56078670-GA-G
• gnomAD v3: 12-55684886-GA-G
• gnomAD v4: 12-55684886-GA-G
• MyVariant Identifiers: chr12:g.56078671del (hg19) ; chr12:g.55684887del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.55684888del , CM000674.2:g.55684888del	GRCh38
NC_000012.11:g.56078672del , CM000674.1:g.56078672del	GRCh37
NC_000012.10:g.54364939del	NCBI36
NG_012343.1:g.32419del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553893.6:c.*3209del	ENSP00000452467.1:n.*3209del
ENST00000554327.6:c.2256del
ENST00000557058.2:n.3000del
ENST00000557555.3:c.3710del	ENSP00000451039.3:n.3710del
ENST00000686981.1:c.*3296del	ENSP00000510795.1:n.*3296del
ENST00000687390.1:n.1691del
ENST00000688413.1:n.2699del
ENST00000691052.1:c.*2069del	ENSP00000508886.1:n.*2069del
ENST00000691846.1:c.2398del
ENST00000691973.1:c.3525del	ENSP00000509141.1:n.3525del
ENST00000257879.11:c.*171del MANE Select	ENSP00000257879.7:n.*171del
ENST00000553804.6:c.*171del	ENSP00000452120.1:n.*171del
ENST00000557555.2:c.788del	ENSP00000451039.2:n.788del
ENST00000257879.10:c.*171del	ENSP00000257879.6:n.*171del
ENST00000347027.10:c.*171del	ENSP00000343009.6:n.*171del
ENST00000452168.6:c.*171del	ENSP00000393844.2:n.*171del
ENST00000553804.5:c.*171del	ENSP00000452120.1:n.*171del
ENST00000554327.5:c.1650del
ENST00000555728.5:c.*171del	ENSP00000452387.1:n.*171del
ENST00000557555.1:c.788del
NM_001144996.1:c.*171del	NP_001138468.1:n.*171del
NM_001144997.1:c.*171del	NP_001138469.1:n.*171del
NM_002206.2:c.*171del	NP_002197.2:n.*171del
XM_005268839.1:c.*171del	XP_005268896.1:n.*171del
XM_005268840.1:c.*171del	XP_005268897.1:n.*171del
XM_005268841.1:c.*341del	XP_005268898.1:n.*341del
XM_005268842.1:c.*171del	XP_005268899.1:n.*171del
XM_005268844.1:c.*171del	XP_005268901.1:n.*171del
XM_005268845.1:c.*171del	XP_005268902.1:n.*171del
XM_005268846.1:c.*171del	XP_005268903.1:n.*171del
XM_005268847.1:c.*171del	XP_005268904.1:n.*171del
XM_005268848.1:c.*171del	XP_005268905.1:n.*171del
XM_005268849.1:c.*171del	XP_005268906.1:n.*171del
XM_005268850.1:c.*171del	XP_005268907.1:n.*171del
XM_011538286.1:c.*171del	XP_011536588.1:n.*171del
XM_005268839.2:c.*171del	XP_005268896.1:n.*171del
XM_005268840.2:c.*171del	XP_005268897.1:n.*171del
XM_005268841.2:c.*341del	XP_005268898.1:n.*341del
XM_005268842.2:c.*171del	XP_005268899.1:n.*171del
XM_017019265.1:c.*171del	XP_016874754.1:n.*171del
NM_001144996.2:c.*171del	NP_001138468.1:n.*171del
NM_001367993.1:c.*171del	NP_001354922.1:n.*171del
NM_001367994.1:c.*171del	NP_001354923.1:n.*171del
NM_001374465.1:c.*171del	NP_001361394.1:n.*171del
NM_002206.3:c.*171del MANE Select	NP_002197.2:n.*171del