Canonical Allele Identifier: CA357402497

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78911390A>T , CM000666.2:g.78911390A>T GRCh38
NC_000004.11:g.79832544A>T , CM000666.1:g.79832544A>T GRCh37
NC_000004.10:g.80051568A>T NCBI36
NG_047162.1:g.140013A>T
NG_053104.1:g.33049T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000502613.3:c.2843A>T (BMP2K) MANE Select ENSP00000424668.2:p.Glu948Val
ENST00000335016.9:c.2843A>T (BMP2K) ENSP00000334836.5:p.Glu948Val
ENST00000342820.10:c.*782+3820T>A (PAQR3) ENSP00000344203.6:n.*782+3820T>A
ENST00000502613.1:c.1920A>T (BMP2K)
ENST00000511594.5:c.*799T>A (PAQR3) ENSP00000425080.1:n.*799T>A
ENST00000512760.5:c.*792+3820T>A (PAQR3) ENSP00000426875.1:n.*792+3820T>A
ENST00000628286.1:c.*1819A>T (BMP2K) ENSP00000487317.1:n.*1819A>T
NM_198892.1:c.2843A>T (BMP2K) NP_942595.1:p.Glu948Val
XM_005263117.1:c.2732A>T (BMP2K) XP_005263174.1:p.Glu911Val
XM_011532101.1:c.2603A>T (BMP2K) XP_011530403.1:p.Glu868Val
XR_938694.1:n.1118-5229T>A (PAQR3)
XM_017008381.1:c.2603A>T (BMP2K) XP_016863870.1:p.Glu868Val
XM_017008382.1:c.1955A>T (BMP2K) XP_016863871.1:p.Glu652Val
XR_938694.3:n.1098-5229T>A (PAQR3)
NM_198892.2:c.2843A>T (BMP2K) MANE Select NP_942595.1:p.Glu948Val