Canonical Allele Identifier: CA258100

Linked Data

ClinVar Variation Id: 18077
ClinVar RCV Id: RCV000019703
dbSNP Id: rs121909539

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.20693753C>G , CM000676.2:g.20693753C>G GRCh38
NC_000014.8:g.21161912C>G , CM000676.1:g.21161912C>G GRCh37
NC_000014.7:g.20231752C>G NCBI36
NG_008717.2:g.14577C>G , LRG_653:g.14577C>G
NG_033053.1:g.14541C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000397990.5:c.189C>G (ANG) MANE Select ENSP00000381077.4:p.Cys63Trp
ENST00000555835.3:c.-17-5602C>G (RNASE4) MANE Select ENSP00000452245.1:n.-17-5602C>G
ENST00000336811.10:c.189C>G (ANG) ENSP00000336762.6:p.Cys63Trp
ENST00000397990.4:c.189C>G (ANG) ENSP00000381077.4:p.Cys63Trp
ENST00000397995.2:c.-17-5602C>G (RNASE4) ENSP00000381081.2:n.-17-5602C>G
ENST00000553909.1:c.86+103C>G ENSP00000477037.1:n.86+103C>G
ENST00000554073.1:n.146-5113C>G (ANG)
ENST00000555597.1:c.-18+4879C>G (RNASE4) ENSP00000451624.1:n.-18+4879C>G
ENST00000555835.2:c.-17-5602C>G (RNASE4) ENSP00000452245.1:n.-17-5602C>G
NM_001097577.2:c.189C>G (ANG) NP_001091046.1:p.Cys63Trp
NM_001145.4:c.189C>G , LRG_653t1:c.189C>G (ANG) NP_001136.1:p.Cys63Trp
NM_001282192.1:c.-18+103C>G (RNASE4) NP_001269121.1:n.-18+103C>G
NM_001282193.1:c.-17-5602C>G (RNASE4) NP_001269122.1:n.-17-5602C>G
NM_002937.4:c.-17-5602C>G (RNASE4) NP_002928.1:n.-17-5602C>G
NM_194431.2:c.-18+4879C>G (RNASE4) NP_919412.1:n.-18+4879C>G
NM_002937.5:c.-17-5602C>G (RNASE4) MANE Select NP_002928.1:n.-17-5602C>G
NM_001097577.3:c.189C>G (ANG) MANE Select NP_001091046.1:p.Cys63Trp
NM_001282192.2:c.-18+103C>G (RNASE4) NP_001269121.1:n.-18+103C>G
NM_001282193.2:c.-17-5602C>G (RNASE4) NP_001269122.1:n.-17-5602C>G
NM_194431.3:c.-18+4879C>G (RNASE4) NP_919412.1:n.-18+4879C>G
NM_001385271.1:c.189C>G (ANG) NP_001372200.1:p.Cys63Trp
NM_001385272.1:c.189C>G (ANG) NP_001372201.1:p.Cys63Trp
NM_001385273.1:c.189C>G (ANG) NP_001372202.1:p.Cys63Trp
NM_001385274.1:c.189C>G (ANG) NP_001372203.1:p.Cys63Trp
NR_174964.1:n.467-4G>C (EGILA)