Canonical Allele Identifier: CA480145497

Gene: ITGA7

Linked Data

• MyVariant Identifiers: chr12:g.56087039A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.55693255A>G , CM000674.2:g.55693255A>G	GRCh38
NC_000012.11:g.56087039A>G , CM000674.1:g.56087039A>G	GRCh37
NC_000012.10:g.54373306A>G	NCBI36
NG_012343.1:g.24051T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553893.6:c.*2222T>C	ENSP00000452467.1:n.*2222T>C
ENST00000554327.6:c.1269T>C
ENST00000557058.2:n.2013T>C
ENST00000557257.2:c.2124T>C	ENSP00000450578.2:p.Pro708=
ENST00000557555.3:c.2610T>C	ENSP00000451039.3:p.Pro870=
ENST00000686981.1:c.*2309T>C	ENSP00000510795.1:n.*2309T>C
ENST00000687390.1:n.704T>C
ENST00000691052.1:c.*1082T>C	ENSP00000508886.1:n.*1082T>C
ENST00000691846.1:c.1411T>C
ENST00000691973.1:c.2610T>C	ENSP00000509141.1:p.Pro870=
ENST00000257879.11:c.2598T>C MANE Select	ENSP00000257879.7:p.Pro866=
ENST00000553804.6:c.2610T>C	ENSP00000452120.1:p.Pro870=
ENST00000257879.10:c.2598T>C	ENSP00000257879.6:p.Pro866=
ENST00000347027.10:c.2580T>C	ENSP00000343009.6:p.Pro860=
ENST00000452168.6:c.2319T>C	ENSP00000393844.2:p.Pro773=
ENST00000553804.5:c.2610T>C	ENSP00000452120.1:p.Pro870=
ENST00000554327.5:c.663T>C
ENST00000555728.5:c.2730T>C	ENSP00000452387.1:p.Pro910=
NM_001144996.1:c.2610T>C	NP_001138468.1:p.Pro870=
NM_001144997.1:c.2319T>C	NP_001138469.1:p.Pro773=
NM_002206.2:c.2598T>C	NP_002197.2:p.Pro866=
XM_005268839.1:c.2730T>C	XP_005268896.1:p.Pro910=
XM_005268840.1:c.2712T>C	XP_005268897.1:p.Pro904=
XM_005268841.1:c.2730T>C	XP_005268898.1:p.Pro910=
XM_005268842.1:c.2580T>C	XP_005268899.1:p.Pro860=
XM_005268844.1:c.2391T>C	XP_005268901.1:p.Pro797=
XM_005268845.1:c.2259T>C	XP_005268902.1:p.Pro753=
XM_005268846.1:c.2259T>C	XP_005268903.1:p.Pro753=
XM_005268847.1:c.2256T>C	XP_005268904.1:p.Pro752=
XM_005268848.1:c.2256T>C	XP_005268905.1:p.Pro752=
XM_005268849.1:c.2256T>C	XP_005268906.1:p.Pro752=
XM_005268850.1:c.2124T>C	XP_005268907.1:p.Pro708=
XM_011538286.1:c.2391T>C	XP_011536588.1:p.Pro797=
XM_005268839.2:c.2730T>C	XP_005268896.1:p.Pro910=
XM_005268840.2:c.2712T>C	XP_005268897.1:p.Pro904=
XM_005268841.2:c.2730T>C	XP_005268898.1:p.Pro910=
XM_005268842.2:c.2580T>C	XP_005268899.1:p.Pro860=
XM_017019265.1:c.2340T>C	XP_016874754.1:p.Pro780=
NM_001144996.2:c.2610T>C	NP_001138468.1:p.Pro870=
NM_001367993.1:c.2271T>C	NP_001354922.1:p.Pro757=
NM_001367994.1:c.1254T>C	NP_001354923.1:p.Pro418=
NM_001374465.1:c.2580T>C	NP_001361394.1:p.Pro860=
NM_002206.3:c.2598T>C MANE Select	NP_002197.2:p.Pro866=