Canonical Allele Identifier: CA221925

Gene: ITGA7

Linked Data

• ClinVar Variation Id: 94040
• ClinVar RCV Id: RCV000723765 ; RCV001080080 ; RCV003935038
• dbSNP Id: rs149081471
• ExAC: 12:56087068 C / T
• gnomAD v2: 12-56087068-C-T
• gnomAD v3: 12-55693284-C-T
• gnomAD v4: 12-55693284-C-T
• MyVariant Identifiers: chr12:g.56087068C>T (hg19) ; chr12:g.55693284C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.55693284C>T , CM000674.2:g.55693284C>T	GRCh38
NC_000012.11:g.56087068C>T , CM000674.1:g.56087068C>T	GRCh37
NC_000012.10:g.54373335C>T	NCBI36
NG_012343.1:g.24022G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553893.6:c.*2193G>A	ENSP00000452467.1:n.*2193G>A
ENST00000554327.6:c.1240G>A
ENST00000557058.2:n.1984G>A
ENST00000557257.2:c.2095G>A	ENSP00000450578.2:p.Gly699Ser
ENST00000557555.3:c.2581G>A	ENSP00000451039.3:p.Gly861Ser
ENST00000686981.1:c.*2280G>A	ENSP00000510795.1:n.*2280G>A
ENST00000687390.1:n.675G>A
ENST00000691052.1:c.*1053G>A	ENSP00000508886.1:n.*1053G>A
ENST00000691846.1:c.1382G>A
ENST00000691973.1:c.2581G>A	ENSP00000509141.1:p.Gly861Ser
ENST00000257879.11:c.2569G>A MANE Select	ENSP00000257879.7:p.Gly857Ser
ENST00000553804.6:c.2581G>A	ENSP00000452120.1:p.Gly861Ser
ENST00000257879.10:c.2569G>A	ENSP00000257879.6:p.Gly857Ser
ENST00000347027.10:c.2551G>A	ENSP00000343009.6:p.Gly851Ser
ENST00000452168.6:c.2290G>A	ENSP00000393844.2:p.Gly764Ser
ENST00000553804.5:c.2581G>A	ENSP00000452120.1:p.Gly861Ser
ENST00000554327.5:c.634G>A
ENST00000555728.5:c.2701G>A	ENSP00000452387.1:p.Gly901Ser
NM_001144996.1:c.2581G>A	NP_001138468.1:p.Gly861Ser
NM_001144997.1:c.2290G>A	NP_001138469.1:p.Gly764Ser
NM_002206.2:c.2569G>A	NP_002197.2:p.Gly857Ser
XM_005268839.1:c.2701G>A	XP_005268896.1:p.Gly901Ser
XM_005268840.1:c.2683G>A	XP_005268897.1:p.Gly895Ser
XM_005268841.1:c.2701G>A	XP_005268898.1:p.Gly901Ser
XM_005268842.1:c.2551G>A	XP_005268899.1:p.Gly851Ser
XM_005268844.1:c.2362G>A	XP_005268901.1:p.Gly788Ser
XM_005268845.1:c.2230G>A	XP_005268902.1:p.Gly744Ser
XM_005268846.1:c.2230G>A	XP_005268903.1:p.Gly744Ser
XM_005268847.1:c.2227G>A	XP_005268904.1:p.Gly743Ser
XM_005268848.1:c.2227G>A	XP_005268905.1:p.Gly743Ser
XM_005268849.1:c.2227G>A	XP_005268906.1:p.Gly743Ser
XM_005268850.1:c.2095G>A	XP_005268907.1:p.Gly699Ser
XM_011538286.1:c.2362G>A	XP_011536588.1:p.Gly788Ser
XM_005268839.2:c.2701G>A	XP_005268896.1:p.Gly901Ser
XM_005268840.2:c.2683G>A	XP_005268897.1:p.Gly895Ser
XM_005268841.2:c.2701G>A	XP_005268898.1:p.Gly901Ser
XM_005268842.2:c.2551G>A	XP_005268899.1:p.Gly851Ser
XM_017019265.1:c.2311G>A	XP_016874754.1:p.Gly771Ser
NM_001144996.2:c.2581G>A	NP_001138468.1:p.Gly861Ser
NM_001367993.1:c.2242G>A	NP_001354922.1:p.Gly748Ser
NM_001367994.1:c.1225G>A	NP_001354923.1:p.Gly409Ser
NM_001374465.1:c.2551G>A	NP_001361394.1:p.Gly851Ser
NM_002206.3:c.2569G>A MANE Select	NP_002197.2:p.Gly857Ser