Canonical Allele Identifier: CA385181781

Gene: ITGA7

Linked Data

• MyVariant Identifiers: chr12:g.56087073G>C (hg19) ; chr12:g.55693289G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.55693289G>C , CM000674.2:g.55693289G>C	GRCh38
NC_000012.11:g.56087073G>C , CM000674.1:g.56087073G>C	GRCh37
NC_000012.10:g.54373340G>C	NCBI36
NG_012343.1:g.24017C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553893.6:c.*2188C>G	ENSP00000452467.1:n.*2188C>G
ENST00000554327.6:c.1235C>G
ENST00000557058.2:n.1979C>G
ENST00000557257.2:c.2090C>G	ENSP00000450578.2:p.Thr697Ser
ENST00000557555.3:c.2576C>G	ENSP00000451039.3:p.Thr859Ser
ENST00000686981.1:c.*2275C>G	ENSP00000510795.1:n.*2275C>G
ENST00000687390.1:n.670C>G
ENST00000691052.1:c.*1048C>G	ENSP00000508886.1:n.*1048C>G
ENST00000691846.1:c.1377C>G
ENST00000691973.1:c.2576C>G	ENSP00000509141.1:p.Thr859Ser
ENST00000257879.11:c.2564C>G MANE Select	ENSP00000257879.7:p.Thr855Ser
ENST00000553804.6:c.2576C>G	ENSP00000452120.1:p.Thr859Ser
ENST00000257879.10:c.2564C>G	ENSP00000257879.6:p.Thr855Ser
ENST00000347027.10:c.2546C>G	ENSP00000343009.6:p.Thr849Ser
ENST00000452168.6:c.2285C>G	ENSP00000393844.2:p.Thr762Ser
ENST00000553804.5:c.2576C>G	ENSP00000452120.1:p.Thr859Ser
ENST00000554327.5:c.629C>G
ENST00000555728.5:c.2696C>G	ENSP00000452387.1:p.Thr899Ser
NM_001144996.1:c.2576C>G	NP_001138468.1:p.Thr859Ser
NM_001144997.1:c.2285C>G	NP_001138469.1:p.Thr762Ser
NM_002206.2:c.2564C>G	NP_002197.2:p.Thr855Ser
XM_005268839.1:c.2696C>G	XP_005268896.1:p.Thr899Ser
XM_005268840.1:c.2678C>G	XP_005268897.1:p.Thr893Ser
XM_005268841.1:c.2696C>G	XP_005268898.1:p.Thr899Ser
XM_005268842.1:c.2546C>G	XP_005268899.1:p.Thr849Ser
XM_005268844.1:c.2357C>G	XP_005268901.1:p.Thr786Ser
XM_005268845.1:c.2225C>G	XP_005268902.1:p.Thr742Ser
XM_005268846.1:c.2225C>G	XP_005268903.1:p.Thr742Ser
XM_005268847.1:c.2222C>G	XP_005268904.1:p.Thr741Ser
XM_005268848.1:c.2222C>G	XP_005268905.1:p.Thr741Ser
XM_005268849.1:c.2222C>G	XP_005268906.1:p.Thr741Ser
XM_005268850.1:c.2090C>G	XP_005268907.1:p.Thr697Ser
XM_011538286.1:c.2357C>G	XP_011536588.1:p.Thr786Ser
XM_005268839.2:c.2696C>G	XP_005268896.1:p.Thr899Ser
XM_005268840.2:c.2678C>G	XP_005268897.1:p.Thr893Ser
XM_005268841.2:c.2696C>G	XP_005268898.1:p.Thr899Ser
XM_005268842.2:c.2546C>G	XP_005268899.1:p.Thr849Ser
XM_017019265.1:c.2306C>G	XP_016874754.1:p.Thr769Ser
NM_001144996.2:c.2576C>G	NP_001138468.1:p.Thr859Ser
NM_001367993.1:c.2237C>G	NP_001354922.1:p.Thr746Ser
NM_001367994.1:c.1220C>G	NP_001354923.1:p.Thr407Ser
NM_001374465.1:c.2546C>G	NP_001361394.1:p.Thr849Ser
NM_002206.3:c.2564C>G MANE Select	NP_002197.2:p.Thr855Ser