Canonical Allele Identifier: CA385181716

Gene: ITGA7

Linked Data

• MyVariant Identifiers: chr12:g.56087043C>A (hg19) ; chr12:g.55693259C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.55693259C>A , CM000674.2:g.55693259C>A	GRCh38
NC_000012.11:g.56087043C>A , CM000674.1:g.56087043C>A	GRCh37
NC_000012.10:g.54373310C>A	NCBI36
NG_012343.1:g.24047G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553893.6:c.*2218G>T	ENSP00000452467.1:n.*2218G>T
ENST00000554327.6:c.1265G>T
ENST00000557058.2:n.2009G>T
ENST00000557257.2:c.2120G>T	ENSP00000450578.2:p.Trp707Leu
ENST00000557555.3:c.2606G>T	ENSP00000451039.3:p.Trp869Leu
ENST00000686981.1:c.*2305G>T	ENSP00000510795.1:n.*2305G>T
ENST00000687390.1:n.700G>T
ENST00000691052.1:c.*1078G>T	ENSP00000508886.1:n.*1078G>T
ENST00000691846.1:c.1407G>T
ENST00000691973.1:c.2606G>T	ENSP00000509141.1:p.Trp869Leu
ENST00000257879.11:c.2594G>T MANE Select	ENSP00000257879.7:p.Trp865Leu
ENST00000553804.6:c.2606G>T	ENSP00000452120.1:p.Trp869Leu
ENST00000257879.10:c.2594G>T	ENSP00000257879.6:p.Trp865Leu
ENST00000347027.10:c.2576G>T	ENSP00000343009.6:p.Trp859Leu
ENST00000452168.6:c.2315G>T	ENSP00000393844.2:p.Trp772Leu
ENST00000553804.5:c.2606G>T	ENSP00000452120.1:p.Trp869Leu
ENST00000554327.5:c.659G>T
ENST00000555728.5:c.2726G>T	ENSP00000452387.1:p.Trp909Leu
NM_001144996.1:c.2606G>T	NP_001138468.1:p.Trp869Leu
NM_001144997.1:c.2315G>T	NP_001138469.1:p.Trp772Leu
NM_002206.2:c.2594G>T	NP_002197.2:p.Trp865Leu
XM_005268839.1:c.2726G>T	XP_005268896.1:p.Trp909Leu
XM_005268840.1:c.2708G>T	XP_005268897.1:p.Trp903Leu
XM_005268841.1:c.2726G>T	XP_005268898.1:p.Trp909Leu
XM_005268842.1:c.2576G>T	XP_005268899.1:p.Trp859Leu
XM_005268844.1:c.2387G>T	XP_005268901.1:p.Trp796Leu
XM_005268845.1:c.2255G>T	XP_005268902.1:p.Trp752Leu
XM_005268846.1:c.2255G>T	XP_005268903.1:p.Trp752Leu
XM_005268847.1:c.2252G>T	XP_005268904.1:p.Trp751Leu
XM_005268848.1:c.2252G>T	XP_005268905.1:p.Trp751Leu
XM_005268849.1:c.2252G>T	XP_005268906.1:p.Trp751Leu
XM_005268850.1:c.2120G>T	XP_005268907.1:p.Trp707Leu
XM_011538286.1:c.2387G>T	XP_011536588.1:p.Trp796Leu
XM_005268839.2:c.2726G>T	XP_005268896.1:p.Trp909Leu
XM_005268840.2:c.2708G>T	XP_005268897.1:p.Trp903Leu
XM_005268841.2:c.2726G>T	XP_005268898.1:p.Trp909Leu
XM_005268842.2:c.2576G>T	XP_005268899.1:p.Trp859Leu
XM_017019265.1:c.2336G>T	XP_016874754.1:p.Trp779Leu
NM_001144996.2:c.2606G>T	NP_001138468.1:p.Trp869Leu
NM_001367993.1:c.2267G>T	NP_001354922.1:p.Trp756Leu
NM_001367994.1:c.1250G>T	NP_001354923.1:p.Trp417Leu
NM_001374465.1:c.2576G>T	NP_001361394.1:p.Trp859Leu
NM_002206.3:c.2594G>T MANE Select	NP_002197.2:p.Trp865Leu