Canonical Allele Identifier: CA2241598898

Gene: ANKRD11

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89275330_89275332delinsAAC , CM000678.2:g.89275330_89275332delinsAAC	GRCh38
NC_000016.9:g.89341738_89341740delinsAAC , CM000678.1:g.89341738_89341740delinsAAC	GRCh37
NC_000016.8:g.87869239_87869241delinsAAC	NCBI36
NG_032003.1:g.220230_220232delinsGTT
NG_032003.2:g.220230_220232delinsGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301030.10:c.7471-141_7471-139delinsGTT MANE Select	ENSP00000301030.4:n.7471-141_7471-139delinsGTT
ENST00000330736.10:c.*7274-141_*7274-139delinsGTT	ENSP00000330815.5:n.*7274-141_*7274-139delinsGTT
ENST00000378330.7:c.7471-141_7471-139delinsGTT	ENSP00000367581.2:n.7471-141_7471-139delinsGTT
ENST00000642600.1:c.7471-141_7471-139delinsGTT	ENSP00000495226.1:n.7471-141_7471-139delinsGTT
ENST00000644285.1:c.745-141_745-139delinsGTT	ENSP00000496476.1:n.745-141_745-139delinsGTT
ENST00000301030.8:c.7471-141_7471-139delinsGTT	ENSP00000301030.4:n.7471-141_7471-139delinsGTT
ENST00000330736.9:c.*7274-141_*7274-139delinsGTT	ENSP00000330815.5:n.*7274-141_*7274-139delinsGTT
ENST00000378330.6:c.7471-141_7471-139delinsGTT	ENSP00000367581.2:n.7471-141_7471-139delinsGTT
ENST00000562194.1:c.152-141_152-139delinsGTT
NM_001256182.1:c.7471-141_7471-139delinsGTT	NP_001243111.1:n.7471-141_7471-139delinsGTT
NM_001256183.1:c.7471-141_7471-139delinsGTT	NP_001243112.1:n.7471-141_7471-139delinsGTT
NM_013275.5:c.7471-141_7471-139delinsGTT	NP_037407.4:n.7471-141_7471-139delinsGTT
XM_006721181.1:c.7369-141_7369-139delinsGTT	XP_006721244.1:n.7369-141_7369-139delinsGTT
XM_006721184.2:c.7174-141_7174-139delinsGTT	XP_006721247.1:n.7174-141_7174-139delinsGTT
XM_011523051.1:c.7471-141_7471-139delinsGTT	XP_011521353.1:n.7471-141_7471-139delinsGTT
XM_011523052.1:c.7471-141_7471-139delinsGTT	XP_011521354.1:n.7471-141_7471-139delinsGTT
XM_011523053.1:c.7471-141_7471-139delinsGTT	XP_011521355.1:n.7471-141_7471-139delinsGTT
XM_011523054.1:c.7369-141_7369-139delinsGTT	XP_011521356.1:n.7369-141_7369-139delinsGTT
XM_011523055.1:c.7369-141_7369-139delinsGTT	XP_011521357.1:n.7369-141_7369-139delinsGTT
XM_011523056.1:c.7342-141_7342-139delinsGTT	XP_011521358.1:n.7342-141_7342-139delinsGTT
XM_011523057.1:c.7471-141_7471-139delinsGTT	XP_011521359.1:n.7471-141_7471-139delinsGTT
XM_011523051.3:c.7471-141_7471-139delinsGTT	XP_011521353.1:n.7471-141_7471-139delinsGTT
XM_011523053.2:c.7471-141_7471-139delinsGTT	XP_011521355.1:n.7471-141_7471-139delinsGTT
XM_011523054.2:c.7369-141_7369-139delinsGTT	XP_011521356.1:n.7369-141_7369-139delinsGTT
XM_011523055.2:c.7369-141_7369-139delinsGTT	XP_011521357.1:n.7369-141_7369-139delinsGTT
XM_011523056.2:c.7342-141_7342-139delinsGTT	XP_011521358.1:n.7342-141_7342-139delinsGTT
XM_011523057.2:c.7471-141_7471-139delinsGTT	XP_011521359.1:n.7471-141_7471-139delinsGTT
XM_017023182.2:c.7471-141_7471-139delinsGTT	XP_016878671.1:n.7471-141_7471-139delinsGTT
XM_017023183.1:c.7471-141_7471-139delinsGTT	XP_016878672.1:n.7471-141_7471-139delinsGTT
XM_017023184.1:c.7471-141_7471-139delinsGTT	XP_016878673.1:n.7471-141_7471-139delinsGTT
XM_017023185.1:c.7471-141_7471-139delinsGTT	XP_016878674.1:n.7471-141_7471-139delinsGTT
XM_017023186.1:c.7471-141_7471-139delinsGTT	XP_016878675.1:n.7471-141_7471-139delinsGTT
XM_017023187.1:c.7471-141_7471-139delinsGTT	XP_016878676.1:n.7471-141_7471-139delinsGTT
XM_024450244.1:c.7369-141_7369-139delinsGTT	XP_024306012.1:n.7369-141_7369-139delinsGTT
NM_013275.6:c.7471-141_7471-139delinsGTT MANE Select	NP_037407.4:n.7471-141_7471-139delinsGTT
NM_001256182.2:c.7471-141_7471-139delinsGTT	NP_001243111.1:n.7471-141_7471-139delinsGTT
NM_001256183.2:c.7471-141_7471-139delinsGTT	NP_001243112.1:n.7471-141_7471-139delinsGTT