Canonical Allele Identifier: CA1148964022

Gene: INTS11

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1320561A= , CM000663.2:g.1320561A=	GRCh38
NC_000001.10:g.1255941A= , CM000663.1:g.1255941A=	GRCh37
NC_000001.9:g.1245804A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435064.6:c.127-32T= MANE Select	ENSP00000413493.2:n.127-32T=
ENST00000323275.10:n.574T=
ENST00000411962.5:c.135+2620T=	ENSP00000400548.1:n.135+2620T=
ENST00000419704.5:c.126+435T=	ENSP00000404886.1:n.126+435T=
ENST00000421495.6:c.-530+4020T=	ENSP00000464436.1:n.-530+4020T=
ENST00000429572.5:c.127-32T=	ENSP00000481275.1:n.127-32T=
ENST00000430786.5:c.*5-32T=	ENSP00000404012.1:n.*5-32T=
ENST00000434694.6:c.127-32T=	ENSP00000411233.2:n.127-32T=
ENST00000435064.5:c.127-32T=	ENSP00000413493.1:n.127-32T=
ENST00000450926.6:c.127-32T=	ENSP00000392848.2:n.127-32T=
ENST00000458452.7:c.*411-32T=	ENSP00000433930.1:n.*411-32T=
ENST00000470679.3:c.243T=
ENST00000488042.6:n.148-32T=
ENST00000490853.5:n.168-32T=
ENST00000493534.6:n.177-32T=
ENST00000496353.1:n.564T=
ENST00000498173.2:n.640T=
ENST00000498476.6:c.307-32T=	ENSP00000436824.1:n.307-32T=
ENST00000525285.1:c.528-32T=
ENST00000525603.1:n.345T=
ENST00000526113.1:n.57+4020T=
ENST00000526332.5:c.-172-1037T=	ENSP00000434790.1:n.-172-1037T=
ENST00000526797.5:c.127-32T=	ENSP00000435418.1:n.127-32T=
ENST00000526904.5:n.78+4020T=
ENST00000527098.5:c.234-32T=	ENSP00000431952.1:n.234-32T=
ENST00000527719.5:c.145-32T=	ENSP00000436743.1:n.145-32T=
ENST00000528879.5:c.127-32T=	ENSP00000432777.1:n.127-32T=
ENST00000530031.5:c.268-32T=	ENSP00000432009.1:n.268-32T=
ENST00000531019.5:c.*77T=	ENSP00000433733.1:n.*77T=
ENST00000532772.5:c.126+435T=	ENSP00000431214.1:n.126+435T=
ENST00000532952.5:n.161-32T=
ENST00000534345.5:c.130-32T=	ENSP00000435772.1:n.130-32T=
ENST00000540437.5:c.145-32T=	ENSP00000445001.1:n.145-32T=
ENST00000545578.5:c.40-32T=	ENSP00000444672.1:n.40-32T=
ENST00000618806.4:c.127-32T=	ENSP00000480957.1:n.127-32T=
ENST00000620829.4:c.139+2616T=	ENSP00000481821.1:n.139+2616T=
NM_001256456.1:c.145-32T=	NP_001243385.1:n.145-32T=
NM_001256460.1:c.40-32T=	NP_001243389.1:n.40-32T=
NM_001256462.1:c.139+2616T=	NP_001243391.1:n.139+2616T=
NM_001256463.1:c.126+435T=	NP_001243392.1:n.126+435T=
NM_017871.5:c.127-32T=	NP_060341.2:n.127-32T=
XM_011541647.1:c.307-32T=	XP_011539949.1:n.307-32T=
XM_011541648.1:c.193-32T=	XP_011539950.1:n.193-32T=
XM_011541649.1:c.307-32T=	XP_011539951.1:n.307-32T=
XM_011541650.1:c.-155-32T=	XP_011539952.1:n.-155-32T=
XM_011541650.2:c.-155-32T=	XP_011539952.1:n.-155-32T=
XM_017001557.1:c.-155-32T=	XP_016857046.1:n.-155-32T=
XM_017001558.1:c.-155-32T=	XP_016857047.1:n.-155-32T=
NM_001256463.2:c.126+435T=	NP_001243392.1:n.126+435T=
NM_017871.6:c.127-32T= MANE Select	NP_060341.2:n.127-32T=
NM_001256456.2:c.145-32T=	NP_001243385.1:n.145-32T=
NM_001256460.2:c.40-32T=	NP_001243389.1:n.40-32T=
NM_001256462.2:c.139+2616T=	NP_001243391.1:n.139+2616T=