Canonical Allele Identifier: CA2485274458
Gene: INTS7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.211981579A= , CM000663.2:g.211981579A= GRCh38
NC_000001.10:g.212154921A= , CM000663.1:g.212154921A= GRCh37
NC_000001.9:g.210221544A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000366994.8:c.1133-389T= MANE Select ENSP00000355961.3:n.1133-389T=
ENST00000366992.7:c.1133-389T= ENSP00000355959.3:n.1133-389T=
ENST00000366993.7:c.1133-389T= ENSP00000355960.3:n.1133-389T=
ENST00000366994.7:c.1133-389T= ENSP00000355961.3:n.1133-389T=
ENST00000440600.6:c.986-389T= ENSP00000388908.2:n.986-389T=
ENST00000469606.5:c.*903-389T= ENSP00000481687.1:n.*903-389T=
NM_001199809.1:c.986-389T= NP_001186738.1:n.986-389T=
NM_001199811.1:c.1133-389T= NP_001186740.1:n.1133-389T=
NM_001199812.1:c.1133-389T= NP_001186741.1:n.1133-389T=
NM_015434.3:c.1133-389T= NP_056249.1:n.1133-389T=
NR_037667.1:n.1390-389T=
XM_011509396.1:c.1133-389T= XP_011507698.1:n.1133-389T=
XM_011509397.1:c.1055-389T= XP_011507699.1:n.1055-389T=
XM_011509396.2:c.1133-389T= XP_011507698.1:n.1133-389T=
XM_017000962.1:c.1133-389T= XP_016856451.1:n.1133-389T=
NM_015434.4:c.1133-389T= MANE Select NP_056249.1:n.1133-389T=
NM_001199809.2:c.986-389T= NP_001186738.1:n.986-389T=
NM_001199811.2:c.1133-389T= NP_001186740.1:n.1133-389T=
NM_001199812.2:c.1133-389T= NP_001186741.1:n.1133-389T=
NR_037667.2:n.1287-389T=