Canonical Allele Identifier: CA385181540

Gene: ITGA7

Linked Data

• MyVariant Identifiers: chr12:g.56086961T>G (hg19) ; chr12:g.55693177T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.55693177T>G , CM000674.2:g.55693177T>G	GRCh38
NC_000012.11:g.56086961T>G , CM000674.1:g.56086961T>G	GRCh37
NC_000012.10:g.54373228T>G	NCBI36
NG_012343.1:g.24129A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553893.6:c.*2300A>C	ENSP00000452467.1:n.*2300A>C
ENST00000554327.6:c.1347A>C
ENST00000557058.2:n.2091A>C
ENST00000557257.2:c.2202A>C	ENSP00000450578.2:p.Lys734Asn
ENST00000557555.3:c.2688A>C	ENSP00000451039.3:p.Lys896Asn
ENST00000686981.1:c.*2387A>C	ENSP00000510795.1:n.*2387A>C
ENST00000687390.1:n.782A>C
ENST00000691052.1:c.*1160A>C	ENSP00000508886.1:n.*1160A>C
ENST00000691846.1:c.1489A>C
ENST00000691973.1:c.2652+36A>C	ENSP00000509141.1:n.2652+36A>C
ENST00000257879.11:c.2676A>C MANE Select	ENSP00000257879.7:p.Lys892Asn
ENST00000553804.6:c.2688A>C	ENSP00000452120.1:p.Lys896Asn
ENST00000257879.10:c.2676A>C	ENSP00000257879.6:p.Lys892Asn
ENST00000347027.10:c.2658A>C	ENSP00000343009.6:p.Lys886Asn
ENST00000452168.6:c.2397A>C	ENSP00000393844.2:p.Lys799Asn
ENST00000553804.5:c.2688A>C	ENSP00000452120.1:p.Lys896Asn
ENST00000554327.5:c.741A>C
ENST00000555728.5:c.2808A>C	ENSP00000452387.1:p.Lys936Asn
NM_001144996.1:c.2688A>C	NP_001138468.1:p.Lys896Asn
NM_001144997.1:c.2397A>C	NP_001138469.1:p.Lys799Asn
NM_002206.2:c.2676A>C	NP_002197.2:p.Lys892Asn
XM_005268839.1:c.2808A>C	XP_005268896.1:p.Lys936Asn
XM_005268840.1:c.2790A>C	XP_005268897.1:p.Lys930Asn
XM_005268841.1:c.2808A>C	XP_005268898.1:p.Lys936Asn
XM_005268842.1:c.2658A>C	XP_005268899.1:p.Lys886Asn
XM_005268844.1:c.2469A>C	XP_005268901.1:p.Lys823Asn
XM_005268845.1:c.2337A>C	XP_005268902.1:p.Lys779Asn
XM_005268846.1:c.2337A>C	XP_005268903.1:p.Lys779Asn
XM_005268847.1:c.2334A>C	XP_005268904.1:p.Lys778Asn
XM_005268848.1:c.2334A>C	XP_005268905.1:p.Lys778Asn
XM_005268849.1:c.2334A>C	XP_005268906.1:p.Lys778Asn
XM_005268850.1:c.2202A>C	XP_005268907.1:p.Lys734Asn
XM_011538286.1:c.2469A>C	XP_011536588.1:p.Lys823Asn
XM_005268839.2:c.2808A>C	XP_005268896.1:p.Lys936Asn
XM_005268840.2:c.2790A>C	XP_005268897.1:p.Lys930Asn
XM_005268841.2:c.2808A>C	XP_005268898.1:p.Lys936Asn
XM_005268842.2:c.2658A>C	XP_005268899.1:p.Lys886Asn
XM_017019265.1:c.2418A>C	XP_016874754.1:p.Lys806Asn
NM_001144996.2:c.2688A>C	NP_001138468.1:p.Lys896Asn
NM_001367993.1:c.2349A>C	NP_001354922.1:p.Lys783Asn
NM_001367994.1:c.1332A>C	NP_001354923.1:p.Lys444Asn
NM_001374465.1:c.2658A>C	NP_001361394.1:p.Lys886Asn
NM_002206.3:c.2676A>C MANE Select	NP_002197.2:p.Lys892Asn