Canonical Allele Identifier: CA385181498

Gene: ITGA7

Linked Data

• MyVariant Identifiers: chr12:g.56086941G>C (hg19) ; chr12:g.55693157G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.55693157G>C , CM000674.2:g.55693157G>C	GRCh38
NC_000012.11:g.56086941G>C , CM000674.1:g.56086941G>C	GRCh37
NC_000012.10:g.54373208G>C	NCBI36
NG_012343.1:g.24149C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553893.6:c.*2320C>G	ENSP00000452467.1:n.*2320C>G
ENST00000554327.6:c.1367C>G
ENST00000557058.2:n.2111C>G
ENST00000557257.2:c.2222C>G	ENSP00000450578.2:p.Pro741Arg
ENST00000557555.3:c.2708C>G	ENSP00000451039.3:p.Pro903Arg
ENST00000686981.1:c.*2407C>G	ENSP00000510795.1:n.*2407C>G
ENST00000687390.1:n.802C>G
ENST00000691052.1:c.*1180C>G	ENSP00000508886.1:n.*1180C>G
ENST00000691846.1:c.1509C>G
ENST00000691973.1:c.2652+56C>G	ENSP00000509141.1:n.2652+56C>G
ENST00000257879.11:c.2696C>G MANE Select	ENSP00000257879.7:p.Pro899Arg
ENST00000553804.6:c.2708C>G	ENSP00000452120.1:p.Pro903Arg
ENST00000257879.10:c.2696C>G	ENSP00000257879.6:p.Pro899Arg
ENST00000347027.10:c.2678C>G	ENSP00000343009.6:p.Pro893Arg
ENST00000452168.6:c.2417C>G	ENSP00000393844.2:p.Pro806Arg
ENST00000553804.5:c.2708C>G	ENSP00000452120.1:p.Pro903Arg
ENST00000554327.5:c.761C>G
ENST00000555728.5:c.2828C>G	ENSP00000452387.1:p.Pro943Arg
NM_001144996.1:c.2708C>G	NP_001138468.1:p.Pro903Arg
NM_001144997.1:c.2417C>G	NP_001138469.1:p.Pro806Arg
NM_002206.2:c.2696C>G	NP_002197.2:p.Pro899Arg
XM_005268839.1:c.2828C>G	XP_005268896.1:p.Pro943Arg
XM_005268840.1:c.2810C>G	XP_005268897.1:p.Pro937Arg
XM_005268841.1:c.2828C>G	XP_005268898.1:p.Pro943Arg
XM_005268842.1:c.2678C>G	XP_005268899.1:p.Pro893Arg
XM_005268844.1:c.2489C>G	XP_005268901.1:p.Pro830Arg
XM_005268845.1:c.2357C>G	XP_005268902.1:p.Pro786Arg
XM_005268846.1:c.2357C>G	XP_005268903.1:p.Pro786Arg
XM_005268847.1:c.2354C>G	XP_005268904.1:p.Pro785Arg
XM_005268848.1:c.2354C>G	XP_005268905.1:p.Pro785Arg
XM_005268849.1:c.2354C>G	XP_005268906.1:p.Pro785Arg
XM_005268850.1:c.2222C>G	XP_005268907.1:p.Pro741Arg
XM_011538286.1:c.2489C>G	XP_011536588.1:p.Pro830Arg
XM_005268839.2:c.2828C>G	XP_005268896.1:p.Pro943Arg
XM_005268840.2:c.2810C>G	XP_005268897.1:p.Pro937Arg
XM_005268841.2:c.2828C>G	XP_005268898.1:p.Pro943Arg
XM_005268842.2:c.2678C>G	XP_005268899.1:p.Pro893Arg
XM_017019265.1:c.2438C>G	XP_016874754.1:p.Pro813Arg
NM_001144996.2:c.2708C>G	NP_001138468.1:p.Pro903Arg
NM_001367993.1:c.2369C>G	NP_001354922.1:p.Pro790Arg
NM_001367994.1:c.1352C>G	NP_001354923.1:p.Pro451Arg
NM_001374465.1:c.2678C>G	NP_001361394.1:p.Pro893Arg
NM_002206.3:c.2696C>G MANE Select	NP_002197.2:p.Pro899Arg