Canonical Allele Identifier: CA385181601

Gene: ITGA7

Linked Data

• MyVariant Identifiers: chr12:g.56086992T>G (hg19) ; chr12:g.55693208T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.55693208T>G , CM000674.2:g.55693208T>G	GRCh38
NC_000012.11:g.56086992T>G , CM000674.1:g.56086992T>G	GRCh37
NC_000012.10:g.54373259T>G	NCBI36
NG_012343.1:g.24098A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553893.6:c.*2269A>C	ENSP00000452467.1:n.*2269A>C
ENST00000554327.6:c.1316A>C
ENST00000557058.2:n.2060A>C
ENST00000557257.2:c.2171A>C	ENSP00000450578.2:p.Glu724Ala
ENST00000557555.3:c.2657A>C	ENSP00000451039.3:p.Glu886Ala
ENST00000686981.1:c.*2356A>C	ENSP00000510795.1:n.*2356A>C
ENST00000687390.1:n.751A>C
ENST00000691052.1:c.*1129A>C	ENSP00000508886.1:n.*1129A>C
ENST00000691846.1:c.1458A>C
ENST00000691973.1:c.2652+5A>C	ENSP00000509141.1:n.2652+5A>C
ENST00000257879.11:c.2645A>C MANE Select	ENSP00000257879.7:p.Glu882Ala
ENST00000553804.6:c.2657A>C	ENSP00000452120.1:p.Glu886Ala
ENST00000257879.10:c.2645A>C	ENSP00000257879.6:p.Glu882Ala
ENST00000347027.10:c.2627A>C	ENSP00000343009.6:p.Glu876Ala
ENST00000452168.6:c.2366A>C	ENSP00000393844.2:p.Glu789Ala
ENST00000553804.5:c.2657A>C	ENSP00000452120.1:p.Glu886Ala
ENST00000554327.5:c.710A>C
ENST00000555728.5:c.2777A>C	ENSP00000452387.1:p.Glu926Ala
NM_001144996.1:c.2657A>C	NP_001138468.1:p.Glu886Ala
NM_001144997.1:c.2366A>C	NP_001138469.1:p.Glu789Ala
NM_002206.2:c.2645A>C	NP_002197.2:p.Glu882Ala
XM_005268839.1:c.2777A>C	XP_005268896.1:p.Glu926Ala
XM_005268840.1:c.2759A>C	XP_005268897.1:p.Glu920Ala
XM_005268841.1:c.2777A>C	XP_005268898.1:p.Glu926Ala
XM_005268842.1:c.2627A>C	XP_005268899.1:p.Glu876Ala
XM_005268844.1:c.2438A>C	XP_005268901.1:p.Glu813Ala
XM_005268845.1:c.2306A>C	XP_005268902.1:p.Glu769Ala
XM_005268846.1:c.2306A>C	XP_005268903.1:p.Glu769Ala
XM_005268847.1:c.2303A>C	XP_005268904.1:p.Glu768Ala
XM_005268848.1:c.2303A>C	XP_005268905.1:p.Glu768Ala
XM_005268849.1:c.2303A>C	XP_005268906.1:p.Glu768Ala
XM_005268850.1:c.2171A>C	XP_005268907.1:p.Glu724Ala
XM_011538286.1:c.2438A>C	XP_011536588.1:p.Glu813Ala
XM_005268839.2:c.2777A>C	XP_005268896.1:p.Glu926Ala
XM_005268840.2:c.2759A>C	XP_005268897.1:p.Glu920Ala
XM_005268841.2:c.2777A>C	XP_005268898.1:p.Glu926Ala
XM_005268842.2:c.2627A>C	XP_005268899.1:p.Glu876Ala
XM_017019265.1:c.2387A>C	XP_016874754.1:p.Glu796Ala
NM_001144996.2:c.2657A>C	NP_001138468.1:p.Glu886Ala
NM_001367993.1:c.2318A>C	NP_001354922.1:p.Glu773Ala
NM_001367994.1:c.1301A>C	NP_001354923.1:p.Glu434Ala
NM_001374465.1:c.2627A>C	NP_001361394.1:p.Glu876Ala
NM_002206.3:c.2645A>C MANE Select	NP_002197.2:p.Glu882Ala