Canonical Allele Identifier: CA389120703

Gene: RNASE4 EGILA

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.20699418C>G , CM000676.2:g.20699418C>G	GRCh38
NC_000014.8:g.21167577C>G , CM000676.1:g.21167577C>G	GRCh37
NC_000014.7:g.20237417C>G	NCBI36
NG_008717.2:g.20242C>G , LRG_653:g.20242C>G
NG_033053.1:g.20206C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000555835.3:c.47C>G (RNASE4) MANE Select	ENSP00000452245.1:p.Thr16Ser
ENST00000397995.2:c.47C>G (RNASE4)	ENSP00000381081.2:p.Thr16Ser
ENST00000553909.1:c.*54C>G	ENSP00000477037.1:n.*54C>G
ENST00000555597.1:c.47C>G (RNASE4)	ENSP00000451624.1:p.Thr16Ser
ENST00000555835.2:c.47C>G (RNASE4)	ENSP00000452245.1:p.Thr16Ser
NM_001282192.1:c.47C>G (RNASE4)	NP_001269121.1:p.Thr16Ser
NM_001282193.1:c.47C>G (RNASE4)	NP_001269122.1:p.Thr16Ser
NM_002937.4:c.47C>G (RNASE4)	NP_002928.1:p.Thr16Ser
NM_194431.2:c.47C>G (RNASE4)	NP_919412.1:p.Thr16Ser
NM_002937.5:c.47C>G (RNASE4) MANE Select	NP_002928.1:p.Thr16Ser
NM_001282192.2:c.47C>G (RNASE4)	NP_001269121.1:p.Thr16Ser
NM_001282193.2:c.47C>G (RNASE4)	NP_001269122.1:p.Thr16Ser
NM_194431.3:c.47C>G (RNASE4)	NP_919412.1:p.Thr16Ser
NR_174964.1:n.276G>C (EGILA)