Canonical Allele Identifier: CA2485274502

Gene: INTS7

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.211981687_211981688delinsGA , CM000663.2:g.211981687_211981688delinsGA	GRCh38
NC_000001.10:g.212155029_212155030delinsGA , CM000663.1:g.212155029_212155030delinsGA	GRCh37
NC_000001.9:g.210221652_210221653delinsGA	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000366994.8:c.1133-498_1133-497delinsTC MANE Select	ENSP00000355961.3:n.1133-498_1133-497deli...
ENST00000366992.7:c.1133-498_1133-497delinsTC	ENSP00000355959.3:n.1133-498_1133-497deli...
ENST00000366993.7:c.1133-498_1133-497delinsTC	ENSP00000355960.3:n.1133-498_1133-497deli...
ENST00000366994.7:c.1133-498_1133-497delinsTC	ENSP00000355961.3:n.1133-498_1133-497deli...
ENST00000440600.6:c.986-498_986-497delinsTC	ENSP00000388908.2:n.986-498_986-497delins...
ENST00000469606.5:c.*903-498_*903-497delinsTC	ENSP00000481687.1:n.*903-498_*903-497deli...
NM_001199809.1:c.986-498_986-497delinsTC	NP_001186738.1:n.986-498_986-497delinsTC
NM_001199811.1:c.1133-498_1133-497delinsTC	NP_001186740.1:n.1133-498_1133-497delinsT...
NM_001199812.1:c.1133-498_1133-497delinsTC	NP_001186741.1:n.1133-498_1133-497delinsT...
NM_015434.3:c.1133-498_1133-497delinsTC	NP_056249.1:n.1133-498_1133-497delinsTC
NR_037667.1:n.1390-498_1390-497delinsTC
XM_011509396.1:c.1133-498_1133-497delinsTC	XP_011507698.1:n.1133-498_1133-497delinsT...
XM_011509397.1:c.1055-498_1055-497delinsTC	XP_011507699.1:n.1055-498_1055-497delinsT...
XM_011509396.2:c.1133-498_1133-497delinsTC	XP_011507698.1:n.1133-498_1133-497delinsT...
XM_017000962.1:c.1133-498_1133-497delinsTC	XP_016856451.1:n.1133-498_1133-497delinsT...
NM_015434.4:c.1133-498_1133-497delinsTC MANE Select	NP_056249.1:n.1133-498_1133-497delinsTC
NM_001199809.2:c.986-498_986-497delinsTC	NP_001186738.1:n.986-498_986-497delinsTC
NM_001199811.2:c.1133-498_1133-497delinsTC	NP_001186740.1:n.1133-498_1133-497delinsT...
NM_001199812.2:c.1133-498_1133-497delinsTC	NP_001186741.1:n.1133-498_1133-497delinsT...
NR_037667.2:n.1287-498_1287-497delinsTC