Canonical Allele Identifier: CA2485274515

Gene: INTS7

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.211981722G= , CM000663.2:g.211981722G=	GRCh38
NC_000001.10:g.212155064G= , CM000663.1:g.212155064G=	GRCh37
NC_000001.9:g.210221687G=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000366994.8:c.1133-532C= MANE Select	ENSP00000355961.3:n.1133-532C=
ENST00000366992.7:c.1133-532C=	ENSP00000355959.3:n.1133-532C=
ENST00000366993.7:c.1133-532C=	ENSP00000355960.3:n.1133-532C=
ENST00000366994.7:c.1133-532C=	ENSP00000355961.3:n.1133-532C=
ENST00000440600.6:c.986-532C=	ENSP00000388908.2:n.986-532C=
ENST00000469606.5:c.*903-532C=	ENSP00000481687.1:n.*903-532C=
NM_001199809.1:c.986-532C=	NP_001186738.1:n.986-532C=
NM_001199811.1:c.1133-532C=	NP_001186740.1:n.1133-532C=
NM_001199812.1:c.1133-532C=	NP_001186741.1:n.1133-532C=
NM_015434.3:c.1133-532C=	NP_056249.1:n.1133-532C=
NR_037667.1:n.1390-532C=
XM_011509396.1:c.1133-532C=	XP_011507698.1:n.1133-532C=
XM_011509397.1:c.1055-532C=	XP_011507699.1:n.1055-532C=
XM_011509396.2:c.1133-532C=	XP_011507698.1:n.1133-532C=
XM_017000962.1:c.1133-532C=	XP_016856451.1:n.1133-532C=
NM_015434.4:c.1133-532C= MANE Select	NP_056249.1:n.1133-532C=
NM_001199809.2:c.986-532C=	NP_001186738.1:n.986-532C=
NM_001199811.2:c.1133-532C=	NP_001186740.1:n.1133-532C=
NM_001199812.2:c.1133-532C=	NP_001186741.1:n.1133-532C=
NR_037667.2:n.1287-532C=