Canonical Allele Identifier: CA385181679

Gene: ITGA7

Linked Data

• MyVariant Identifiers: chr12:g.56087026T>G (hg19) ; chr12:g.55693242T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.55693242T>G , CM000674.2:g.55693242T>G	GRCh38
NC_000012.11:g.56087026T>G , CM000674.1:g.56087026T>G	GRCh37
NC_000012.10:g.54373293T>G	NCBI36
NG_012343.1:g.24064A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553893.6:c.*2235A>C	ENSP00000452467.1:n.*2235A>C
ENST00000554327.6:c.1282A>C
ENST00000557058.2:n.2026A>C
ENST00000557257.2:c.2137A>C	ENSP00000450578.2:p.Asn713His
ENST00000557555.3:c.2623A>C	ENSP00000451039.3:p.Asn875His
ENST00000686981.1:c.*2322A>C	ENSP00000510795.1:n.*2322A>C
ENST00000687390.1:n.717A>C
ENST00000691052.1:c.*1095A>C	ENSP00000508886.1:n.*1095A>C
ENST00000691846.1:c.1424A>C
ENST00000691973.1:c.2623A>C	ENSP00000509141.1:p.Asn875His
ENST00000257879.11:c.2611A>C MANE Select	ENSP00000257879.7:p.Asn871His
ENST00000553804.6:c.2623A>C	ENSP00000452120.1:p.Asn875His
ENST00000257879.10:c.2611A>C	ENSP00000257879.6:p.Asn871His
ENST00000347027.10:c.2593A>C	ENSP00000343009.6:p.Asn865His
ENST00000452168.6:c.2332A>C	ENSP00000393844.2:p.Asn778His
ENST00000553804.5:c.2623A>C	ENSP00000452120.1:p.Asn875His
ENST00000554327.5:c.676A>C
ENST00000555728.5:c.2743A>C	ENSP00000452387.1:p.Asn915His
NM_001144996.1:c.2623A>C	NP_001138468.1:p.Asn875His
NM_001144997.1:c.2332A>C	NP_001138469.1:p.Asn778His
NM_002206.2:c.2611A>C	NP_002197.2:p.Asn871His
XM_005268839.1:c.2743A>C	XP_005268896.1:p.Asn915His
XM_005268840.1:c.2725A>C	XP_005268897.1:p.Asn909His
XM_005268841.1:c.2743A>C	XP_005268898.1:p.Asn915His
XM_005268842.1:c.2593A>C	XP_005268899.1:p.Asn865His
XM_005268844.1:c.2404A>C	XP_005268901.1:p.Asn802His
XM_005268845.1:c.2272A>C	XP_005268902.1:p.Asn758His
XM_005268846.1:c.2272A>C	XP_005268903.1:p.Asn758His
XM_005268847.1:c.2269A>C	XP_005268904.1:p.Asn757His
XM_005268848.1:c.2269A>C	XP_005268905.1:p.Asn757His
XM_005268849.1:c.2269A>C	XP_005268906.1:p.Asn757His
XM_005268850.1:c.2137A>C	XP_005268907.1:p.Asn713His
XM_011538286.1:c.2404A>C	XP_011536588.1:p.Asn802His
XM_005268839.2:c.2743A>C	XP_005268896.1:p.Asn915His
XM_005268840.2:c.2725A>C	XP_005268897.1:p.Asn909His
XM_005268841.2:c.2743A>C	XP_005268898.1:p.Asn915His
XM_005268842.2:c.2593A>C	XP_005268899.1:p.Asn865His
XM_017019265.1:c.2353A>C	XP_016874754.1:p.Asn785His
NM_001144996.2:c.2623A>C	NP_001138468.1:p.Asn875His
NM_001367993.1:c.2284A>C	NP_001354922.1:p.Asn762His
NM_001367994.1:c.1267A>C	NP_001354923.1:p.Asn423His
NM_001374465.1:c.2593A>C	NP_001361394.1:p.Asn865His
NM_002206.3:c.2611A>C MANE Select	NP_002197.2:p.Asn871His