Canonical Allele Identifier: CA2122156389

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.20690751G= , CM000676.2:g.20690751G= GRCh38
NC_000014.8:g.21158910G= , CM000676.1:g.21158910G= GRCh37
NC_000014.7:g.20228750G= NCBI36
NG_008717.2:g.11575G= , LRG_653:g.11575G=
NG_033053.1:g.11539G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000397990.5:c.-19+1877G= (ANG) MANE Select ENSP00000381077.4:n.-19+1877G=
ENST00000555835.3:c.-18+5993G= (RNASE4) MANE Select ENSP00000452245.1:n.-18+5993G=
ENST00000336811.10:c.-18-2796G= (ANG) ENSP00000336762.6:n.-18-2796G=
ENST00000397990.4:c.-19+1877G= (ANG) ENSP00000381077.4:n.-19+1877G=
ENST00000397995.2:c.-18+6055G= (RNASE4) ENSP00000381081.2:n.-18+6055G=
ENST00000553909.1:c.-18-2796G= ENSP00000477037.1:n.-18-2796G=
ENST00000554073.1:n.145+5993G= (ANG)
ENST00000555597.1:c.-18+1877G= (RNASE4) ENSP00000451624.1:n.-18+1877G=
ENST00000555835.2:c.-18+5993G= (RNASE4) ENSP00000452245.1:n.-18+5993G=
NM_001097577.2:c.-19+1877G= (ANG) NP_001091046.1:n.-19+1877G=
NM_001145.4:c.-18-2796G= , LRG_653t1:c.-18-2796G= (ANG) NP_001136.1:n.-18-2796G=
NM_001282192.1:c.-121-2796G= (RNASE4) NP_001269121.1:n.-121-2796G=
NM_001282193.1:c.-18+6055G= (RNASE4) NP_001269122.1:n.-18+6055G=
NM_002937.4:c.-18+5993G= (RNASE4) NP_002928.1:n.-18+5993G=
NM_194431.2:c.-18+1877G= (RNASE4) NP_919412.1:n.-18+1877G=
NM_002937.5:c.-18+5993G= (RNASE4) MANE Select NP_002928.1:n.-18+5993G=
NM_001097577.3:c.-19+1877G= (ANG) MANE Select NP_001091046.1:n.-19+1877G=
NM_001282192.2:c.-121-2796G= (RNASE4) NP_001269121.1:n.-121-2796G=
NM_001282193.2:c.-18+6055G= (RNASE4) NP_001269122.1:n.-18+6055G=
NM_194431.3:c.-18+1877G= (RNASE4) NP_919412.1:n.-18+1877G=
NM_001385271.1:c.-142-2280G= (ANG) NP_001372200.1:n.-142-2280G=
NM_001385272.1:c.-140+1877G= (ANG) NP_001372201.1:n.-140+1877G=
NM_001385273.1:c.-18-2796G= (ANG) NP_001372202.1:n.-18-2796G=
NM_001385274.1:c.-19+1896G= (ANG) NP_001372203.1:n.-19+1896G=