Canonical Allele Identifier: CA480145459

Gene: ITGA7

Linked Data

• MyVariant Identifiers: chr12:g.56087027G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.55693243G>A , CM000674.2:g.55693243G>A	GRCh38
NC_000012.11:g.56087027G>A , CM000674.1:g.56087027G>A	GRCh37
NC_000012.10:g.54373294G>A	NCBI36
NG_012343.1:g.24063C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553893.6:c.*2234C>T	ENSP00000452467.1:n.*2234C>T
ENST00000554327.6:c.1281C>T
ENST00000557058.2:n.2025C>T
ENST00000557257.2:c.2136C>T	ENSP00000450578.2:p.Ala712=
ENST00000557555.3:c.2622C>T	ENSP00000451039.3:p.Ala874=
ENST00000686981.1:c.*2321C>T	ENSP00000510795.1:n.*2321C>T
ENST00000687390.1:n.716C>T
ENST00000691052.1:c.*1094C>T	ENSP00000508886.1:n.*1094C>T
ENST00000691846.1:c.1423C>T
ENST00000691973.1:c.2622C>T	ENSP00000509141.1:p.Ala874=
ENST00000257879.11:c.2610C>T MANE Select	ENSP00000257879.7:p.Ala870=
ENST00000553804.6:c.2622C>T	ENSP00000452120.1:p.Ala874=
ENST00000257879.10:c.2610C>T	ENSP00000257879.6:p.Ala870=
ENST00000347027.10:c.2592C>T	ENSP00000343009.6:p.Ala864=
ENST00000452168.6:c.2331C>T	ENSP00000393844.2:p.Ala777=
ENST00000553804.5:c.2622C>T	ENSP00000452120.1:p.Ala874=
ENST00000554327.5:c.675C>T
ENST00000555728.5:c.2742C>T	ENSP00000452387.1:p.Ala914=
NM_001144996.1:c.2622C>T	NP_001138468.1:p.Ala874=
NM_001144997.1:c.2331C>T	NP_001138469.1:p.Ala777=
NM_002206.2:c.2610C>T	NP_002197.2:p.Ala870=
XM_005268839.1:c.2742C>T	XP_005268896.1:p.Ala914=
XM_005268840.1:c.2724C>T	XP_005268897.1:p.Ala908=
XM_005268841.1:c.2742C>T	XP_005268898.1:p.Ala914=
XM_005268842.1:c.2592C>T	XP_005268899.1:p.Ala864=
XM_005268844.1:c.2403C>T	XP_005268901.1:p.Ala801=
XM_005268845.1:c.2271C>T	XP_005268902.1:p.Ala757=
XM_005268846.1:c.2271C>T	XP_005268903.1:p.Ala757=
XM_005268847.1:c.2268C>T	XP_005268904.1:p.Ala756=
XM_005268848.1:c.2268C>T	XP_005268905.1:p.Ala756=
XM_005268849.1:c.2268C>T	XP_005268906.1:p.Ala756=
XM_005268850.1:c.2136C>T	XP_005268907.1:p.Ala712=
XM_011538286.1:c.2403C>T	XP_011536588.1:p.Ala801=
XM_005268839.2:c.2742C>T	XP_005268896.1:p.Ala914=
XM_005268840.2:c.2724C>T	XP_005268897.1:p.Ala908=
XM_005268841.2:c.2742C>T	XP_005268898.1:p.Ala914=
XM_005268842.2:c.2592C>T	XP_005268899.1:p.Ala864=
XM_017019265.1:c.2352C>T	XP_016874754.1:p.Ala784=
NM_001144996.2:c.2622C>T	NP_001138468.1:p.Ala874=
NM_001367993.1:c.2283C>T	NP_001354922.1:p.Ala761=
NM_001367994.1:c.1266C>T	NP_001354923.1:p.Ala422=
NM_001374465.1:c.2592C>T	NP_001361394.1:p.Ala864=
NM_002206.3:c.2610C>T MANE Select	NP_002197.2:p.Ala870=