Canonical Allele Identifier: CA2200991109

Gene: AXIN1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.342395_342402delinsGACGACTA , CM000678.2:g.342395_342402delinsGACGACTA	GRCh38
NC_000016.9:g.392395_392402delinsGACGACTA , CM000678.1:g.392395_392402delinsGACGACTA	GRCh37
NC_000016.8:g.332396_332403delinsGACGACTA	NCBI36
NG_012267.1:g.15063_15070delinsTAGTCGTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262320.8:c.878+3746_878+3753delinsTAGTCGTC MANE Select	ENSP00000262320.3:n.878+3746_878+3753delinsTAGTCGTC
ENST00000262320.7:c.878+3746_878+3753delinsTAGTCGTC	ENSP00000262320.3:n.878+3746_878+3753delinsTAGTCGTC
ENST00000354866.7:c.878+3746_878+3753delinsTAGTCGTC	ENSP00000346935.3:n.878+3746_878+3753delinsTAGTCGTC
ENST00000461023.5:n.175+3746_175+3753delinsTAGTCGTC
ENST00000481769.1:n.305+9967_305+9974delinsTAGTCGTC
NM_003502.3:c.878+3746_878+3753delinsTAGTCGTC	NP_003493.1:n.878+3746_878+3753delinsTAGTCGTC
NM_181050.2:c.878+3746_878+3753delinsTAGTCGTC	NP_851393.1:n.878+3746_878+3753delinsTAGTCGTC
XM_011522682.1:c.1025+3746_1025+3753delinsTAGTCGTC	XP_011520984.1:n.1025+3746_1025+3753delinsTAGTCGTC
XM_011522683.1:c.1025+3746_1025+3753delinsTAGTCGTC	XP_011520985.1:n.1025+3746_1025+3753delinsTAGTCGTC
XM_011522684.1:c.878+3746_878+3753delinsTAGTCGTC	XP_011520986.1:n.878+3746_878+3753delinsTAGTCGTC
XM_011522685.1:c.62+12656_62+12663delinsTAGTCGTC	XP_011520987.1:n.62+12656_62+12663delinsTAGTCGTC
XM_011522687.1:c.62+12656_62+12663delinsTAGTCGTC	XP_011520989.1:n.62+12656_62+12663delinsTAGTCGTC
XM_011522688.1:c.-1120+3746_-1120+3753delinsTAGTCGTC	XP_011520990.1:n.-1120+3746_-1120+3753delinsTAGTCGTC
NR_134879.1:n.1267+3746_1267+3753delinsTAGTCGTC
XM_011522682.2:c.1025+3746_1025+3753delinsTAGTCGTC	XP_011520984.1:n.1025+3746_1025+3753delinsTAGTCGTC
XM_011522683.2:c.1025+3746_1025+3753delinsTAGTCGTC	XP_011520985.1:n.1025+3746_1025+3753delinsTAGTCGTC
XM_011522684.2:c.878+3746_878+3753delinsTAGTCGTC	XP_011520986.1:n.878+3746_878+3753delinsTAGTCGTC
XM_017023743.1:c.1025+3746_1025+3753delinsTAGTCGTC	XP_016879232.1:n.1025+3746_1025+3753delinsTAGTCGTC
XM_017023744.1:c.1025+3746_1025+3753delinsTAGTCGTC	XP_016879233.1:n.1025+3746_1025+3753delinsTAGTCGTC
XM_017023747.1:c.1025+3746_1025+3753delinsTAGTCGTC	XP_016879236.1:n.1025+3746_1025+3753delinsTAGTCGTC
XM_017023748.1:c.1025+3746_1025+3753delinsTAGTCGTC	XP_016879237.1:n.1025+3746_1025+3753delinsTAGTCGTC
XR_001751996.1:n.1280+3746_1280+3753delinsTAGTCGTC
NM_003502.4:c.878+3746_878+3753delinsTAGTCGTC MANE Select	NP_003493.1:n.878+3746_878+3753delinsTAGTCGTC
NM_181050.3:c.878+3746_878+3753delinsTAGTCGTC	NP_851393.1:n.878+3746_878+3753delinsTAGTCGTC
NR_134879.2:n.1314+3746_1314+3753delinsTAGTCGTC