Canonical Allele Identifier: CA2677350551
Gene: EDN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.12296367_12296372dup , CM000668.2:g.12296367_12296372dup GRCh38
NC_000006.11:g.12296600_12296605dup , CM000668.1:g.12296600_12296605dup GRCh37
NC_000006.10:g.12404586_12404591dup NCBI36
NG_016196.1:g.11072_11077dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000379375.6:c.*300_*305dup MANE Select ENSP00000368683.5:n.*300_*305dup
ENST00000379375.5:c.*300_*305dup ENSP00000368683.5:n.*300_*305dup
NM_001168319.1:c.*300_*305dup NP_001161791.1:n.*300_*305dup
NM_001955.4:c.*300_*305dup NP_001946.3:n.*300_*305dup
XM_011514330.1:c.*300_*305dup XP_011512632.1:n.*300_*305dup
XM_011514331.1:c.*300_*305dup XP_011512633.1:n.*300_*305dup
XM_011514332.1:c.*300_*305dup XP_011512634.1:n.*300_*305dup
XM_011514330.2:c.*300_*305dup XP_011512632.1:n.*300_*305dup
XM_011514331.3:c.*300_*305dup XP_011512633.1:n.*300_*305dup
XM_011514332.2:c.*300_*305dup XP_011512634.1:n.*300_*305dup
XM_017010331.1:c.*300_*305dup XP_016865820.1:n.*300_*305dup
NM_001955.5:c.*300_*305dup MANE Select NP_001946.3:n.*300_*305dup
NM_001168319.2:c.*300_*305dup NP_001161791.1:n.*300_*305dup