Canonical Allele Identifier: CA36820027
Gene: INTS7 HGNC NCBI

Linked Data

dbSNP Id: rs969424921

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.211981717C>A , CM000663.2:g.211981717C>A GRCh38
NC_000001.10:g.212155059C>A , CM000663.1:g.212155059C>A GRCh37
NC_000001.9:g.210221682C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000366994.8:c.1133-527G>T MANE Select ENSP00000355961.3:n.1133-527G>T
ENST00000366992.7:c.1133-527G>T ENSP00000355959.3:n.1133-527G>T
ENST00000366993.7:c.1133-527G>T ENSP00000355960.3:n.1133-527G>T
ENST00000366994.7:c.1133-527G>T ENSP00000355961.3:n.1133-527G>T
ENST00000440600.6:c.986-527G>T ENSP00000388908.2:n.986-527G>T
ENST00000469606.5:c.*903-527G>T ENSP00000481687.1:n.*903-527G>T
NM_001199809.1:c.986-527G>T NP_001186738.1:n.986-527G>T
NM_001199811.1:c.1133-527G>T NP_001186740.1:n.1133-527G>T
NM_001199812.1:c.1133-527G>T NP_001186741.1:n.1133-527G>T
NM_015434.3:c.1133-527G>T NP_056249.1:n.1133-527G>T
NR_037667.1:n.1390-527G>T
XM_011509396.1:c.1133-527G>T XP_011507698.1:n.1133-527G>T
XM_011509397.1:c.1055-527G>T XP_011507699.1:n.1055-527G>T
XM_011509396.2:c.1133-527G>T XP_011507698.1:n.1133-527G>T
XM_017000962.1:c.1133-527G>T XP_016856451.1:n.1133-527G>T
NM_015434.4:c.1133-527G>T MANE Select NP_056249.1:n.1133-527G>T
NM_001199809.2:c.986-527G>T NP_001186738.1:n.986-527G>T
NM_001199811.2:c.1133-527G>T NP_001186740.1:n.1133-527G>T
NM_001199812.2:c.1133-527G>T NP_001186741.1:n.1133-527G>T
NR_037667.2:n.1287-527G>T